Request for Quotation

CT Scanner system < 64 slices/revolution

1

System

I. General Requirements: - Manufacturing year: 2026 or later, brand new - Origin of main machine system: From G7 countries - Main machine system must be fully compatible - Manufacturer must meet ISO 13485, CE, or equivalent standards - Power supply: 380/480V; 50/60Hz - Operating environment requirements: + Maximum temperature ≥ 25°C + Maximum humidity ≥ 80% II. Configuration Requirements: 1. Main machine system includes: - Imaging gantry (including shell, probe array, rotation axis, X-ray source, high voltage power supply, X-ray control): 1 unit - Patient table: 1 set - Control console: 1 set 2. Software and clinical applications that are compatible with the system: 1 set 3. Auxiliary devices included: - Phantom and phantom adjustment stand: 1 set - Patient cushion, table pad: 1 set - Patient fixation device: 1 set - Head support: 1 set - Two-way intercom: 1 set - User manual: 1 set 4. Other accessories: - Contrast agent syringe: 1 unit - 3kVA online UPS for control machine: 1 set - Dry film printer: 1 unit - Three-phase input power cabinet for the system, including circuit breakers, relays, fuse holders, grounding bars, neutral: 1 set - Patient monitor and observation screen: 1 set III. Detailed Requirements: 1. Gantry - Gantry diameter: ≥ 750mm - Maximum rotation speed: ≤ 0.8s - Number of slices: ≥ 32/rotation - Gantry tilt angle: ≥ 30 degrees in both directions - Field of view (FOV): ≥ 400mm 2. Patient table - Up and down movement: ≤ 450mm - ≥ 1,000mm - Imaging range: ≥ 1,200mm - Table movement speed during imaging: ≥ 100mm/s - Maximum load capacity: ≥ 180kg 3. High voltage/X-ray tube - Tube heat capacity: ≥ 2MHU - Maximum positive cooling rate: ≥ 335kHU/min - Focal spot size: ≥ (0.8x1.1) mm - Power: ≥ 24kW - Minimum tube voltage: ≤ 80kV - Maximum tube voltage: ≥ 130kV - Tube current: ≤ 10 - ≥ 220mA 4. Detector - Number of detectors: ≥ 32 rows - Total number of scintillation crystals: ≥ 24,000 - Type: Solid state 5. Imaging modes a. Positioning imaging: Maximum imaging range: ≥ 1,500mm b. Standard imaging: Maximum speed: ≤ 0.8 seconds/rotation Minimum slice thickness: ≤ 0.625mm Maximum slice thickness: ≥ 10mm c. Spiral imaging: Maximum speed: ≤ 0.8 seconds/rotation Minimum slice thickness: ≤ 0.625mm Maximum slice thickness: ≥ 10mm Maximum number of scans: ≥ 100 d. Dynamic imaging: Maximum speed: ≤ 0.8 seconds/rotation Minimum slice thickness: ≤ 0.625mm Maximum slice thickness: ≥ 10mm 6. Main machine control console and display screen: - 24-inch monitor: 1 unit - Display matrix: ≥ (1920 x 1200) - Operating system: Windows - Rendering matrix: ≥ (512 x 512) - Gray scale display: ≥ 256 levels - Refresh rate: ≥ 15 frames/second - Windowing: + WW/WL adjustment + Contrast inversion (black/white) - Image display processing: + Zoom, rotation + Left/right reversal + Multi-slice image addition + Cine imaging, subtraction/addition + Enhanced/smoothing - Image analysis processing: + Distance measurement, angle measurement, volume calculation + CT value measurement + ROI setting - 3D image display: + MPR (SAG, COR, OBL, CURVE, SPINE) + MIP, MinIP, RaySum display + Surface rendering + Volume rendering (VT method) + Perspective view 7. Software and clinical applications that are compatible with the system, including: - Image reproduction software/function with improved reproduction speed ≥ 50% - Use of image reproduction technology to obtain enhanced contrast images and reduce the amount of contrast agent required for injection - Automatic dose optimization software to adjust based on patient shape and size - Software to reduce metal artifacts - Energy saving software - Image reconstruction and 3D processing software - Data duplication imaging software - Optimization processing software - Automatic MPR software - Software for creating vertebral column images: allows setting MPR slices for curved structures such as the spine - Emergency imaging software - Software for pediatric imaging, minimizing radiation dose for children - Automatic voice command - DICOM connection and standard - Remote fault diagnosis and repair software - Post-scan dose reporting software - Software to export scan reports to PACS system - Software to reduce motion artifacts due to bowel movement - Software to automatically image based on contrast agent absorption threshold - Software for synchronizing the trajectory of the tube before and after imaging with contrast agent, especially in non-contrast imaging - Virtual airway and blood vessel visualization software using contrast agent 8. Dry film printer - Technology: laser or equivalent; - Number of film trays: ≥ 02 trays; - Printing capacity: ≥ 80 films/hour (with 14” x 17” film size); - Film sizes used: 35 x 43 cm, 26 x 36 cm, 25 x 30 cm, 20 x 25 cm - Resolution: ≥ 500 dpi; - DICOM connection. IV. Other Requirements: - Warranty period: ≥ 12 months - X-ray tube: warranty ≥ 12 months or ≥ 50,000 tube shots, whichever comes first

Quang Nam Mental Hospital

Brand new, manufactured in 2026 or later. Complies with the regulations for medical device management as stipulated in Decree 98/2021/ND-CP and amended Decree 07/2023/ND-CP. The contractor is responsible for coordinating with the software operator to fully configure and connect the device to the hospital's HIS (Hospital Information System) and EMR (Electronic Medical Record) systems before commissioning.

General digital X-ray

1

Machine

I. General Requirements: - Year of manufacture: 2026 or later - Machine quality: 100% new - Origin from G7 countries or owners from G7 countries - Synchronized with the manufacturer's system or the manufacturer - Meets quality standards: ISO 13485 or equivalent - Power supply: 3-phase, 380/400 VAC, 50Hz II. Configuration Requirements: - High-frequency power generator and control cabinet: 1 unit - Patient table with 4-way movement: 1 unit - Chest X-ray imaging device: 1 unit - Collimator: 1 unit - X-ray tube: 1 unit - Beam alignment system: 1 set - Fixed flat detector: 2 units - Control and image acquisition workstation: 1 set - Dedicated control and processing software: 1 set - Dry film printer: 1 unit - User manual (English + Vietnamese): 1 set III. Technical Requirements: 1. X-ray generator and control system: - Maximum power output: ≥ 50 kW - kV range: ≤ 40 kV to ≥ 150 kV - mA range: ≤ 10 mA to ≥ 630 mA - mAs range: ≤ 1 mAs to ≥ 500 mAs - Anatomical imaging program: ≥ 1000 anatomical imaging techniques 2. Patient table: - 4-way movable table - Table size: ≥ (75 x 200) cm - Vertical table movement range: ≥ 77 cm - Horizontal table movement range: ≥ 22 cm - Table load capacity: ≥ 300 kg 3. Chest X-ray imaging device: - Column height: ≥ 200 cm - Minimum distance from detector support center to floor: ≥ 300 mm - Maximum distance from detector support center to floor: ≤ 2,000 mm 4. Collimator: - Vertical stand height (from focal spot to floor): ≤ 50 cm to ≥ 180 cm - Longitudinal table movement: ≥ 180 cm - Side arm movement: ≥ 20 cm - Column rotation: ≥ ± 90° - Tube rotation around side arm: ≥ ± 135° - Braking system: Electromagnetic brake 5. X-ray tube: - Maximum voltage: ≥ 150 kV - Anode heat capacity: ≥ 300 kHU 6. Beam alignment system: - Maximum field at SID = 100 cm: ≥ (43 x 43) cm - Main filter: ≤ 2 mm Al 7. Flat detector: - Type: Flat panel - Imaging technology: Charge-coupled device (CCD) - Detector size: ≥ 14” x 17” - Pixel matrix: ≥ 2,300 x 2,800 pixels - Pixel size: ≤ 150μm - Analog conversion: ≥ 16 bit - Meets water resistance standards - Has antibacterial properties 8. Control and image acquisition workstation: - Computer: Intel Core i3 ≥ 3.0 GHz or equivalent, RAM ≥ 8GB, storage drive ≥ 500GB - Workstation monitor: ≥ 17” touch screen - Operating system: Windows 10 or later, with license - Accessories: Keyboard and mouse 9. Software features: - DICOM communication: DICOM image printing, DICOM storage, connection to hospital PACS system - ≥ 300,000 patient ID information storage - Patient information input and protection function - Image processing tools: Contrast/density adjustment, image rotation/flipping, etc. - Image quality inspection function: Display selected images - Breast X-ray positioning function - Intelligent image quality inspection function: S/L value warning - Function to count IP usage managed by barcode scanner 10. Dry film printer: - Technology: Laser or equivalent - Number of film trays: ≥ 2 trays - Printing capacity: ≥ 80 films/hour (for 14” x 17” film size) - Film sizes: 35 x 43 cm, 26 x 36 cm, 25 x 30 cm, 20 x 25 cm - Resolution: ≥ 500 dpi - DICOM connectivity IV. Other Requirements: - Warranty period: ≥ 12 months

Quang Nam Mental Hospital

Brand new, manufactured in 2026 or later. Complies with the regulations for medical device management as stipulated in Decree 98/2021/ND-CP and amended Decree 07/2023/ND-CP. The contractor is responsible for coordinating with the software operator to fully configure and connect the device to the hospital's HIS (Hospital Information System) and EMR (Electronic Medical Record) systems before commissioning.

4D/03 ultrasound probe

1

Machine

I. General Requirements – 100% new machine manufactured after 2026 – Meets quality standards: ISO 13485 – Power supply: 100~120 VAC / 200~240 VAC, 50/60Hz – Maximum power: ≥ 750 VA – Manufacturer and probe origin: from G7 countries II. Configuration Requirements – Main machine body: 1 unit, including: + Display screen: ≥ 21 inches + Touchscreen ≥ 10 inches + Main machine body: ≥ 4 online probe ports: – Convex probe: 1 piece – Linear probe: 1 piece – Sector probe: 1 piece – DICOM network software: 1 piece – High-sensitivity blood vessel imaging software: 1 piece – Dedicated monochrome printer: 1 unit – 2kVa online UPS: 1 unit – English and Vietnamese user manual: 1 set III. Technical Requirements 1. General Information – Includes software/functions to enhance signal from tissue and improve image quality. – Includes AI software/function to enhance images. – Includes automatic whole-image focusing function without manual focus adjustment, which improves resolution or image sensitivity. – Can be upgraded to perform applications: Software/Function for quantitative elastography and ATT assessment of liver fat – Other connection ports: + USB port: ≥ 5 ports – Storage: SSD and HDD hard drive 2. Patient Information and Graphics Display – Patient information input area: ID, name, age, gender, … – Includes a virtual keyboard on the screen – Automatic annotation labeling: ≥ 800 words – Body marking: ≥ 35 types for each area – Probe marking: ≥ 4 types 3. Data Management 3.1 Image Data – Format: – Dynamic/clip images: + DICOM (Raw, MJPEG) + PC format (AVI, WMV, MP4) – Static images: + DICOM (uncompressed, RLE, RGB, JPEG) + PC format (TIFF, BMP, JPEG) – Acquisition mode: – Simultaneous acquisition of RAW image and standard image – RAW image data: maximum ≥ 150s – Standard image data: maximum ≥ 180s – Image management tools: – Displays stored images in thumbnail form with up to ≥ 35 images – Includes check marks on transmitted images – Zoom, rotate, and negative image 4. Storage Capacity – Storage within the main machine: Approximately 500GB – Ability to store via external memory and through hospital network according to DICOM standard 5. Scanning Method – Convex electronic – Convex – Linear electronic – Linear – Phase-array, sector – Radial electronic (2-sided scan) 6. Operating Modes – B mode – Two-plane mode – M mode – Doppler spectrum – Dual-flow Doppler – Color Doppler – Power Doppler – eFLOW mode – High sensitivity color flow imaging mode 7. Image Display Mode – Gray scale B mode: 1 frame, 2 frames, 4 frames – M mode – B and M mode – Doppler spectrum D mode – B and D mode – Color B mode: 1 frame, 2 frames, 4 frames – Energy B mode: 1 frame, 2 frames, 4 frames – High resolution color flow eFlow: 1 frame, 2 frames, 4 frames – DFI mode: 1 frame, 2 frames, 4 frames – B and other modes with 2 Doppler windows: color flow, energy, eFlow – Display 3 mode: B, color flow and real-time Doppler – Display 3 mode: B, energy and real-time Doppler – Display 3 mode: B, DFI and real-time Doppler – Display 3 mode: B, high resolution color flow and real-time Doppler – Image Doppler of tissue – Two-plane image display 8. Electron Beam: – CPWG (Create multi-directional wave) – Programmable wave form transmission/reception – Harmonic wave reception: – Receiving frequency: ≤ 1.0- ≥ 18.0 MHz – Acoustic speed adjustment: ≥ 25 steps – Convergence: – Transmission: Up to ≥ 4 stages of focused transmission – Reception: Focus point System dynamic range: ≥ 270 dB – System processing channel: ≥ 570000 channels – Frame rate: Maximum ≥ 650 frames / second 9. Operating Modes – B mode – M mode – Doppler spectrum – Color Doppler – Power Doppler – High resolution color flow Doppler – High sensitivity blood flow imaging mode 10. Measurement and Analysis: 10.1 Basic Measurements – B mode – M mode – D mode – B/D mode 10.2 Application Measurement Packages 10.2.1 Obstetrics measurements – Support for multiple pregnancies – Growth analysis function (displays historical measurement data) – B mode – Gestational age, fetal weight – Ratio – Amniotic fluid index (AFI), AF Pocket / AFV, MVP CTAR / CTR – Cervical length – M mode – Fetal heart rate – LV function 10.2.2 Gynecology measurements – B mode – Uterus measurement – Intramural uterine wall thickness measurement – Cervix measurement – Ovary measurement – Nipple-mass distance measurement – Thyroid volume measurement – Thyroid sensitivity measurement 10.2.3 Urinary system measurements – B mode – Urine volume – PSA volume – Bladder volume 10.2.4 Vascular measurements – B mode – CCA (Common carotid artery) + ICA (Internal carotid artery) + ECA (External carotid artery) + Bifurcation of the carotid artery + Vertebral artery + Stenotic ratio: + % Area stenosis + % Diameter stenosis – Lower limb vein measurement – Upper limb vein measurement – Stenotic ratio: + % Area stenosis + % Diameter stenosis – Shunt measurement 10.2.5 Abdominal measurements – B mode – Gallbladder measurement – Common bile duct measurement – Liver measurement – Pancreas measurement – Bile duct measurement – Kidney measurement – Spleen measurement – Spatial occupation measurement – Blood vessel diameter measurement – Percentage of stenosis measurement 10.2.6 Small organ measurements – B mode – Tumor measurement – Coagulation distance measurement – Nipple-mass distance measurement – Thyroid volume measurement – Thyroid sensitivity measurement 11. Reporting Functions – Obstetrics report – Gynecology report – Cardiac function report – Vascular report + IMT (Intima-Media Thickness) report – Urinary system report – Abdominal measurement report – Small organ report – Can display past measurement data in the report – Measurement history can be drawn on the report – Can print each report with PC printer option – Can export measured values 12. Doppler Function – Dual window support – Supports PW/PW, TDI/TDI and PW/TDI combinations – Automatic sampling port setting for each port 13. Probe Types 13.1 Convex probe – Frequency range: ≤ 1- ≥ 5.0 MHz – Scan angle: ≥ 70 degrees – Number of elements: ≥ 160 – Application: Fetal, abdominal, pediatric, small organ, … 13.2 Linear probe – Frequency range: ≤ 2 - ≥ 12 MHz – Field of view: ≥ 35mm – Number of elements: ≥ 190 – Application: Abdominal, pediatric, small organ, musculoskeletal, peripheral vascular… 13.3 Sector probe – Frequency range: ≤ 1 - ≥ 5.0 MHz – Scan angle: ≥ 90 degrees – Number of elements: ≥ 60 – Application: Adult heart, peripheral vascular… IV. Other Requirements – Warranty: ≥ 12 months

Quang Nam Mental Hospital

Brand new, manufactured in 2026 or later. Complies with the regulations for medical device management as stipulated in Decree 98/2021/ND-CP and amended Decree 07/2023/ND-CP. The contractor is responsible for coordinating with the software operator to fully configure and connect the device to the hospital's HIS (Hospital Information System) and EMR (Electronic Medical Record) systems before commissioning.

Dual-channel analog multimeter

1

Machine

I. General Requirements: - The device must be manufactured from 2026 onwards, and in new condition (100%). - The manufacturer must have one of the following international certifications: ISO 13485. - Origin: G7 or Europe - Power supply voltage: 220-230V, 50/60Hz - Operating environment conditions: - Maximum temperature: ≥35°C - Maximum humidity: ≥85% II. Configuration Requirements: - Main unit: 1 - Standard accessories: 1 set - User manual (English and Vietnamese): 1 set - Software license: 1 - Desktop computer: 1 set III. Technical Specifications: - The device must meet international EMG monitoring standards - Immediate results display with high quality - Support for ≥50 types of electromyography and EP-guided electrical stimulation techniques: + NCS, EMG, repetitive stimulation, jitter, Estimated number of motor units (MUNE), blink reflex, sacral reflex, bulbocavernous reflex, T wave, Galvanic skin response, Body sensation, visual, auditory, proprioceptive, perception (SEP, VEP, AEP, VEMP, P300, MMN, CNV,…) - All integrated into a compact device - Integrated stimulator, channel, intelligent display and separate control - Software: + Provide various default templates for research on motor and sensory conduction in nerve stimulation. Able to simultaneously record motor and sensory responses. + Can use shortcut keys to switch between response acquisition and F-wave recording modes + Includes a support window with visual representation of the recorded location, background, and stimulating electrodes. + Easily manage the acquisition of short, medium, and long latency electrical potentials using software. + Reports can be easily edited and customized as needed. 1. Main unit: - Interface: USB or better - Safety: BF type 2. Amplifier - Number of channels: ≥2 - Input voltage: 20 µV - 150 mV - Allowable input voltage range tolerance: ±15% for +20 µV to 100 µV: ± 15% + 0.1 to 150 mV: ± 5% - Input capacitance (general): ≤ 30 pF - DC offset compensation (+300 ± 30 mV): Yes - EP range: 0.1 - 400 µV - Allowable EP measurement voltage tolerance range: 4 to 400 µV - Input impedance: ≥ 1 GΩ - Input noise level (20 Hz to 10 000 Hz RMS): ≤ 0.5 μV - High-pass filter: ≥ 23 kHz - Low-pass filter: ≥ 17 kHz - Notch filters for 50/60 Hz (switchable): ≥ 40 dB - Common mode noise reduction at 50 Hz: ≥ 100 dB - Scan rate: 0.1 - 400 ms - Sensitivity: 0.01- 100 mV 3. Stimulator - Number of channels: ≥ 1 - Number of outputs: ≥ 2 - Stimulation amplitude: 0.01 - 100 mA - Stimulation duration: 0.1 - 5 ms - Frequency of repetitive stimulation: 0.1 - 100 Hz - Frequency of chain stimulation: 20 - 500 Hz + Number of stimulations in train:: from 2 - 255 - Paired stimulation + time between pulses: : 20 - 500 ms 4. Integrated auditory stimulator - Stimulation level: 0 - 132 dB - Stimulation frequency: 0.1 - 100 Hz - Tone stimulation + duration: 0.1 - 100 ms - Click stimulation + duration: 0.1 - 5 ms 5. Auditory – visual stimulator - Stimulation level: 0–137 dB - Stimulation frequency: 0.1 - 100 Hz - Tone stimulation + duration: 1–90 ms - Click stimulation + duration: : 10–1000 µs 6. Optical stimulator - Maximum LED brightness: (1100±110) cd/m2 - Stimulation duration: 2 – 1500 ms - Stimulation frequency: 0,1 – 100 Hz 7. Sample stimulator - Stimulation frequency : 0.1 – 10 Hz - Sample size : ≥ 4 samples 8. Control computer - Screen: LCD ≥ 17 inch - CPU: Minimum Core i5 or higher - RAM: ≥ 8GB - SSD: ≥ 512 GB - Software: Windows 10 or higher IV. Other Requirements: - Warranty period: ≥ 12 months - Delivery time: 90 days at the user's location - Installation and testing must be performed by qualified engineers immediately after delivery. - Personnel training: on installation, operation, and maintenance of the device until proficiency is achieved. - In case of any incident, technical staff will arrive within 48 hours to resolve it. - Commitment to provide consumables and spare parts for 8 years. - Must have a valid manufacturer's authorization to supply equipment in Vietnam or a valid representative's authorization in Vietnam. - Must have a regular maintenance plan according to the manufacturer's regulations. - Provide a comprehensive maintenance and repair quotation after the warranty period. - Request quotes for consumables and spare parts. - Commitment that goods meet legal requirements according to Decree 98/2021/ND-CP and related laws.

Quang Nam Mental Hospital

Brand new, manufactured in 2026 or later. Complies with the regulations for medical device management as stipulated in Decree 98/2021/ND-CP and amended Decree 07/2023/ND-CP. The contractor is responsible for coordinating with the software operator to fully configure and connect the device to the hospital's HIS (Hospital Information System) and EMR (Electronic Medical Record) systems before commissioning.

Patient bed (no bar)

20

Female

I. General Requirements: * 100% New Product * Manufacturing Year: 2026 or later * ISO 13485 Compliant II. Configuration Details: 1. Patient Bed Frame: 1 unit 2. Patient Bed Headboard: 2 units 3. Bedside Rails: 2 units III. Technical Specifications: * Bed Size (DxWxH): 1980x930x540±10mm * Material: SUS 304 Stainless Steel * Frame: Constructed from 30x60x0.8mm stainless steel box profile. * Headboard: Constructed from 31.8mm diameter, 0.8mm thick stainless steel tube, with two horizontal support tubes made of 22x0.6mm stainless steel pipe and ten vertical supports made of 15.8 x 0.6 mm stainless steel (each bed has 10 vertical supports). The headboard is assembled to the bed frame using a 2.5mm thick stainless steel panel, with a locking mechanism. * Headboard Height: One end at 800mm high, with a 0.5mm thick stainless steel profile for document holders, and the other end at 900mm high. Rubber feet are attached to the bottom of the headboard. * Bed Base: Consists of two parts: * A 560mm long adjustable head and backrest section with a 25x25x0.6mm stainless steel frame, featuring twelve evenly spaced 10x40x0.4mm stainless steel bars welded to the frame. The angle can be adjusted from 0-45 degrees using a ratcheting mechanism with 2mm thick teeth for increased stability. * The remaining part is the fixed bed base, welded to the frame, featuring thirteen evenly spaced 10x40x0.4mm stainless steel bars, also welded to the frame along with four 25x25x0.6mm stainless steel bars. * Bedside Rails: U-shaped, made of 15.8 x 0.6mm stainless steel tube. * The bed is securely assembled and easy to use. IV. Other Requirements: * Warranty Period: ≥ 12 months * Delivery Time: 90 days at the user's location. * Installation and Testing: Must be performed by qualified engineers with sufficient experience immediately after delivery. * Personnel Training: Provide training on installation, testing, operation, and maintenance of the equipment until proficiency is achieved. * Technical Support: Technical staff must be available within 48 hours to resolve any issues. * Spare Parts Guarantee: Commitment to provide consumable materials and spare parts for a period of 8 years. * Legal Authorization: Must have a valid authorization from the manufacturer allowing supply in Vietnam, or a legal representative's authorization in Vietnam. * Maintenance Plan: Implement a regular maintenance plan according to the manufacturer's specifications during the warranty period. * Comprehensive Maintenance Quotation: Provide a comprehensive maintenance quotation after the warranty period expires. * Request for Quotation: Request quotations for consumable materials and spare parts. * Compliance Guarantee: Guarantee that the products comply with all legal requirements as stipulated in Decree 98/2021/ND-CP and other relevant laws.

Quang Nam Mental Hospital

Brand new, manufactured in 2026 (or later). Complies with the regulations for medical device management as stipulated in Decree 98/2021/ND-CP and amended Decree 07/2023/ND-CP.

Patient bed (with side rails)

10

Female

I. General Requirements: * 100% New Product * Manufacturing Year: 2026 or later * ISO 13485 Compliant II. Configuration Requirements: 1. Patient Bed Frame: 1 unit 2. Patient Bed Headboard: 2 units 3. Bedside Rails: 2 units III. Technical Specifications: * Bed Size (DxWxH): 1980x930x540±10mm * Material: 304 Stainless Steel * Bed Frame: Constructed from 30x60x0.8mm stainless steel box profile. * Headboard: Constructed from 31.8mm diameter, 0.8mm thick stainless steel tube, with a horizontal support bar made of 22x0.6mm stainless steel tube and two vertical supports made of 15.8 x 0.6 mm stainless steel (each bed has 10 vertical supports). The headboard is assembled to the bed frame using a tapered joint. The tapered joint is made from approximately 2mm thick stainless steel sheet, while the tapered joint is made from 3mm thick stainless steel sheet. * Headboard (One End): 800mm high with a 0.5mm thick stainless steel plate for attaching medical records, the other end is 900mm high. Rubber footrests are installed at the bottom of the headboard. * Bed Base: Consists of two parts: * A 560mm long adjustable head and backrest section with a 25x25x0.8mm stainless steel frame, with 12 evenly spaced 10x40x0.4mm stainless steel bars welded to the frame, which can be adjusted from 0-70 degrees using a screw mechanism. * The remaining part is the fixed bed body, which is welded to the frame and has 13 evenly spaced 10x40x0.4mm stainless steel bars, which are reinforced with four 25x25x0.6mm stainless steel bars attached to the bed frame. * One-Handed Adjustment: A single handwheel at the end of the bed. * Bedside Rails: U-shaped, made from 15.8 x 0.6mm diameter stainless steel. * The bed has four 125mm diameter wheels. * The bed is securely welded and assembled for easy use. IV. Other Requirements: * Warranty Period: ≥ 12 months * Delivery Time: 90 days at the user's location. * Installation and Testing: Must be performed immediately after delivery by qualified engineers with sufficient experience. * Personnel Training: Provide training on installation, testing, operation, and maintenance of equipment until proficiency is achieved. * Technical Support: Technical staff must respond within 48 hours in case of any issues. * Spare Parts Guarantee: Commitment to provide consumable materials and spare parts for a period of 8 years. * Legal Authorization: Must have a valid authorization letter from the manufacturer allowing supply of equipment in Vietnam, or a legal representative's authorization letter in Vietnam. * Maintenance Plan: Implement a regular maintenance plan according to the manufacturer's regulations during the warranty period. * Comprehensive Maintenance Quotation: Provide a comprehensive maintenance quotation after the warranty period expires. * Request for Quotations: Request quotations for consumable materials and spare parts. * Compliance Guarantee: Guarantee that the products comply with all legal requirements as stipulated in Decree 98/2021/ND-CP and other relevant laws.

Quang Nam Mental Hospital

Brand new, manufactured in 2026 (or later). Complies with the regulations for medical device management as stipulated in Decree 98/2021/ND-CP and amended Decree 07/2023/ND-CP.

3-lead ECG monitor / 12-lead ECG

1

Machine

I. General Requirements: * Equipment manufactured after 2026, brand new, 100% functional. * Manufacturer has ISO 13485 and FDA certifications. * Origin: From developed countries in the G7 group. * Power supply: 100-240V ±10% AC, 50/60Hz. * Operating environment: * Maximum temperature: ≥30°C * Maximum humidity: ≥75% II. Equipment Configuration * Main unit: 1 * Standard accessories: 1 set * User manual (English and Vietnamese): 1 set III. Technical Specifications: * Superior performance with features comparable to high-end devices, widely used in clinics, health centers, hospitals, and laboratories for reliable results. * Easy to use. * LCD screen: ≥5.1 inch, high resolution, adjustable brightness and contrast, resolution ≥ 800×480. * High-durability silicone keypad for easy operation. * Lithium rechargeable battery with working time of ≥2.5 hours. * External connection ports: SD card, USB. * Result management solution. * Storage up to ≥20 folders. * Unlimited storage on SD card. * ECG: ECG analysis program for adults and children. * Signal acquisition: Acquisition of 12 standard lead signals simultaneously. * A/D converter: ≥24 bits. * Sampling rate: ≥8,000 samples/second. * Frequency response: 0.05 Hz~250 Hz. * Common noise filtering index: >115dB. * Polarization voltage: ±500 mV. * Input signal filtering: Isolation. * Input impedance: ≥50 MΩ. * Input CIR current: ≤0.1 μA. * Patient leakage current: <10 μA. * Constant time: ≥3.2 seconds. * Noise level: ≤12.5 μVp-p. * Threshold voltage sensitivity: ≤20 μV. * Calibration voltage: 1 mV ±3%. * Noise filtering mode settings: EMG noise filtering: 25/35/75/100/150/250Hz, baseline filtering: 0.01/0.02/0.05/0.35/0.5/0.8Hz, AC filtering: 50Hz, 60Hz. * Heart rate range: 30~300 bpm. * Signal acquisition time: 10~24 seconds. Standard Software * Measurement parameters: HR, PR, QRS duration, QT/QTC, P/QRS/T axis, RV5/SV1 amplitude, RV5+SV1 amplitude. * DEMO mode: Standard ECG, Arrhythmia ECG. * QT interval formulas: Bazett, Fridericia, Framingham, Hodges. * Data format: ECG, DICOM, XML, JPEG, PDF. * External connection: Patient cable connection, two USB ports, LAN network connection port. IV. Other Requirements: * Warranty period: ≥12 months. * Delivery time: 90 days at the user's location. * Installation and testing must be performed immediately after delivery by qualified engineers with sufficient experience. * Personnel training: Installation, operation, maintenance, and proficiency in using the equipment. * Technical staff will respond within 48 hours to resolve any issues. * Commitment to providing consumables and spare parts for up to 8 years. * Legitimate manufacturer authorization or a legal representative's authorization in Vietnam is required. * Regular maintenance plan according to the manufacturer's regulations during the warranty period. * Provide comprehensive maintenance and repair quotes after the warranty period. * Request quotes for consumables and spare parts. * Guarantee that the equipment meets all legal requirements as stipulated in Decree 98/2021/ND-CP and related laws.

Quang Nam Mental Hospital

Brand new, manufactured in 2026 or later. Complies with the regulations for medical device management as stipulated in Decree 98/2021/ND-CP and amended Decree 07/2023/ND-CP. The contractor is responsible for coordinating with the software operator to fully configure and connect the device to the hospital's HIS (Hospital Information System) and EMR (Electronic Medical Record) systems before commissioning.

The water filtration system with reverse osmosis (RO) technology has a daily output capacity of 1000 liters.

1

System

I. General Requirements: * Manufacturing Year: 2026 and later * Quality: 100% New * ISO 13485 Quality Standard Compliance * Power Supply: 220VAC ± 10%; 50/60Hz II. Configuration Requirements: * Source Water Tank: 1 set * Pre-filter and Accessories: 1 set * Multi-Media Filter: 1 set * Activated Carbon Filter: 1 set * Water Softener: 1 set * 5 Micron Membrane Filter: 1 set * High Pressure RO Pump: 1 set * RO Reverse Osmosis Column: 1 set * RO Machine Power Control Panel: 1 set * RO Final Water Quality Measurement and Control Device: 1 set * Automatic Control Cabinet: 1 set * RO Water Tank: 1 set * Ozone Generator: 1 set * UV Disinfection Lamp: 1 set * Microbial Filter: 1 set * Stainless Steel Mounting Frame: 1 set III. Technical Specifications: 1. RO Water Tank: * Material: SUS 304 or better stainless steel * Capacity: ≥1000 liters 2. Pre-filter and Accessories: * Pump: Horizontal centrifugal pump with cast iron body and stainless steel impeller (or better) * Power: ≥ 0.55kW (0.75 HP) 3. Multi-Media Filter: * Filter Housing: ANSI/NSF or better standard * Filter Media: ISO 9001 or better quality standard * Automatic Cleaning Washdown Valve: 1 set * Location: Top of the filter column * Flow Rate: ≥ 2m3/h 4. Activated Carbon Filter: * Filter Housing: Composite/Fiberclass or better material * Pressure: ≥ 100 Psi * Filter Media: ISO 9001 or better quality standard 5. Water Softener: * Filter Housing: Composite/Fiberclass or better material * Pressure: ≥ 100 Psi * Filter Media: ISO 9001 or better quality standard 6. Membrane Filter: (Specify membrane type and specifications) 7. High Pressure Pump: * Pump: 1 set, multi-stage centrifugal pump with vertical shaft, cast iron motor, and stainless steel 304 pump body * Power: ≥ 1.1kW (1.5HP) 8. RO Reverse Osmosis Column: * Membrane: NSF or equivalent standard 9. Technical Specification Display Panel: (Specify display type and information displayed) 10. RO Final Product Water Quality Measurement and Control Device 11. Automatic Control Cabinet 12. RO Water Tank: * Material: SUS 304 or better stainless steel * Capacity: ≥500 liters 13. Ozone Generator: * Power: ≥2000mg/h 14. UV Disinfection Lamp 15. Microbial Filter IV. Other Requirements: * Warranty Period: ≥ 12 months * Delivery Time: 90 days at the user's location * Installation and Testing: Must be performed by qualified engineers with sufficient experience immediately after handover. * Personnel Training: Provide training on installation, testing, operation, and maintenance until proficiency is achieved. * Technical Support: Technical staff must be available within 48 hours to resolve any issues. * Spare Parts Guarantee: Commitment to provide consumable materials and spare parts for a period of 8 years. * Legal Authorization: Must have a valid authorization letter from the manufacturer allowing supply in Vietnam, or a legal representative's authorization letter at the time of delivery. * Maintenance Plan: Adhere to the manufacturer's maintenance schedule during the warranty period. * Comprehensive Maintenance Quotation: Provide a comprehensive quotation for maintenance and repair services after the warranty period expires. * Spare Parts Quotation: Request quotations for spare parts. * Compliance with Regulations: Guarantee that all goods comply with the requirements of Decree 98/2021/ND-CP and other relevant legal documents.

Quang Nam Mental Hospital

Brand new, manufactured in 2026 (or later). Complies with the regulations for medical device management as stipulated in Decree 98/2021/ND-CP and amended Decree 07/2023/ND-CP.

50-liter steam sterilization pot

2

Female

1. General Requirements: - Year of Manufacture: 2026 and later - Quality: 100% new - Meets ISO 9001 or equivalent quality management standards - Power Supply: 220V, 50/60Hz - Operating Environment: + Maximum Temperature: ≥ 40 oC + Maximum Humidity: ≥ 75% 2. Configuration Requirements: - Main Unit: 1 unit - Standard Accessories: 1 set - User Manual (English & Vietnamese): 1 set 3. Technical Specifications: - Microprocessor Control System - Liquid Sterilization Program - Specifically designed for hospitals, medical, and laboratory use... - Selectable Sterilization Program - Safety Features: + Overheat Protection + Overpressure Protection + Automatic Door Lock (Pressure) + Emergency Stop Button + Program Reset Button - Automatic Water Supply System - Material: 304 Stainless Steel Chamber and Autoclave Lid - Capacity: ≥ 50 liters - Sterilization Time: Adjustable from 0 – 60 minutes - Sterilization Temperature: 121 oC and 134 oC - Drying Function: Automatic drying, adjustable drying time - Display: LED display or equivalent - Indicators: Power, Heating, Sterilization, Drying, Completion, Overheat. Door closed, low water level, error indication - Water Consumption per Cycle: 700 – 900 cc - Power Consumption: ≤ 2900W / 13 Apm - Heating Power: ≥ 2300W - Drying Power: ≤ 600W 4. Other Requirements: - Warranty Period: ≥ 12 months - Delivery Time: 90 days at the user's location - Installation and Testing: Must be performed by qualified engineers immediately after handover. - Personnel Training: On installation, testing, operation, and maintenance of the equipment until proficiency is achieved. - Technical staff will respond within 48 hours in case of any issues. - Commitment to provide consumables and spare parts for up to 8 years. - Legitimate manufacturer's authorization or legal representative's authorization in Vietnam. - Regular maintenance plan during the warranty period according to the manufacturer's regulations. - Provide a comprehensive maintenance and repair quotation after the warranty period. - Request quotations for consumables and spare parts. - Commitment that the goods comply with the requirements of Decree 98/2021/ND-CP and related legal documents.

Quang Nam Mental Hospital

Brand new, manufactured in 2026 (or later). Complies with the regulations for medical device management as stipulated in Decree 98/2021/ND-CP and amended Decree 07/2023/ND-CP.

The stimulating machine from the skull

2

System

I. General Requirements: * Equipment must be manufactured from 2026 onwards, completely new. * The manufacturer must have one of the following international certifications: ISO 13485. * Origin: G7 or Europe. * Power supply voltage: 220-240V/50-60Hz. * Operating environment conditions: * Operating temperature: ≥ 30°C. * Operating humidity: ≥ 75%. II. Configuration Requirements: * Main unit: 1 system. * Cooling block: 1 piece. * Standard accessories: 1 set. * Patient treatment chair: 1 piece. * Coil winding trolley with support: 1 piece. * Copyrighted software: 1 set. * User manual (English + Vietnamese): 1 set. * Electrical accessories: 1 set. * Computer configuration: 1 set. III. Technical Specifications: * Display: LCD or better. * Stimulation power consumption: * Main unit: ≤ 3000 VA. * Additional power supply: ≤ 3000 VA. * Irbis cooling block: ≤ 1000 VA. * Cooling pad: ≤ 190 VA. * Wireless connection with computer: Wi-Fi, IEEE 802.11b/g/n standard. * Connection to computer: USB or better. * Safety class: I, BF type. Stimulation parameters: * Pulse wave: Biphase. * Pulse duration: 240…410 µs. * Maximum magnetic field: 2.5T. * Rated energy in the main unit at a 100% amplitude setting: 320 J. * Stimulation modes: Single pulse, train, burst, ramp, frequency sweep. * Maximum frequency: 100 Hz. * Maximum pulse frequency in Burst mode: 2000 Hz. * Surface temperature of the stimulating coil to automatically stop the machine: (39 ± 2)°C. * Amplitude range: 0 – 100%. * Intensity (% of movement threshold): 0 – 150%. * Automatic stimulation duration: 1-60 minutes. Train mode: * Pulse frequency in a pulse sequence: + 0.1 – 30 Hz. * Number of pulses in a sequence: 1 – 2000. * Maximum duration: 6000s. * Time between sequences: 0 – 600 s. * Number of sequences in a treatment session: 1 ~ 1000. Burst mode: * Pulse frequency: 10 – 100 Hz. * Number of pulses: 2 – 10. Ramp mode: * Up/down ramp time: 0.1 – 60 s. * Holding/Plateau (horizontal ramp) time: 1 – 600 s. * Pulse frequency in a sequence: 1 – 30 Hz. * Time between sequences: 0 – 600 s. * Number of sequences in each session: 1 – 1000. Sweep mode: * Maximum pulse frequency in a sequence: 1 – 30 Hz. * Starting frequency in a sequence: 1 – 30 Hz. * Up sweep time: 0.1 – 60 s. * Down sweep time: 0.1 – 60 s. * Plateau (horizontal sweep) time: 1 – 600 s. * Time between sequences: 0 – 600 s. Irbis cooling system: * Coolant: PDMS-5 or equivalent. * Cooling fluid pressure in the cooling system: ≤ 0.35 MPa. Trigger input/output synchronization: * Number of trigger inputs: ≥ 1. * Connection type: BNC. * Input impedance: ≥ 47 kΩ. * Minimum input pulse duration: ≥ 100 µs. * Relative input signal triggering delay: 0 – 100 ms. * Allowable relative trigger signal deviation: ± 10%. Control computer: * Display: LCD, minimum ≥ 15 inch. * CPU: Minimum Intel Core i5. * RAM: ≥ 8GB. * SSD: ≥ 512 GB. * Software: Windows 10 (licensed). * Mouse, keyboard. System features: * Wi-Fi connection to other smart devices for power delivery, allowing: * Pre-programmed treatment protocols that can be installed and stored up to 5 protocols in the machine's internal memory and can be modified on the front control screen or via a Wi-Fi app. * New stimulation types: to reduce the "adaptation" of the agent to stimulation. Cooling system: Included. Software: * User manual in Vietnamese, making it easier and simpler to use. * The software provides a large number of pre-installed treatment/rehabilitation protocols with more than 20 different diseases: * Depression. * Obsessive-compulsive disorder (OCD). * Stroke. * Neuropathic pain. * Non-neuropathic pain. * Fibromyalgia. * Visceral pain. * Parkinson's disease. * Schizophrenia. * Tourette's syndrome. * Motor evoked potential (MEP). * Sensory threshold (MT). * Central motor conduction time (CMCT). * Cerebral cortex silent period (CSP). * Corpus callosum (adjacent to CSP). * Paired Associative Stimulation (PAS). * Temporal subcortical inhibition (SAI). * Long-term subcortical inhibition (LAI). * Triple Stimulation Test (TST). * Assessment of central and peripheral motor pathways in adults and children. * Assessment of neurological cranial functions. * Early diagnosis, evaluation, prognosis, and monitoring of multiple sclerosis, movement disorders, neurodegenerative diseases, spinal cord injury. IV. Other Requirements: * Warranty period: ≥ 12 months. * Delivery time: 90 days at the user's location. * Installation and testing must be performed immediately after delivery by qualified engineers. * Personnel training: on installation, operation, and maintenance of the equipment until proficiency is achieved. * In case of any incident, technical staff will be present within 48 hours to resolve it. * Commitment to providing consumables and spare parts for a period of 8 years. * Must have a valid manufacturer's authorization allowing the supply of equipment in Vietnam or a valid representative's authorization in Vietnam. * Must have a regular maintenance plan according to the manufacturer's regulations. * Provide a comprehensive maintenance and repair quotation after the warranty period. * Request quotes for consumables and spare parts. * Comply with all legal requirements as stipulated in Decree 98/2021/ND-CP and related laws.

Quang Nam Mental Hospital

Brand new, manufactured in 2026 or later. Complies with the regulations for medical device management as stipulated in Decree 98/2021/ND-CP and amended Decree 07/2023/ND-CP. The contractor is responsible for coordinating with the software operator to fully configure and connect the device to the hospital's HIS (Hospital Information System) and EMR (Electronic Medical Record) systems before commissioning.