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Intubation light set with camera

1

Female

I. General Requirements - 100% new equipment, manufactured from 2026 onwards - Manufacturer must meet ISO 13485 and CE or ISO 13485 and FDA standards - Origin requirements: Complete and legal Certificate of Origin (CO) and Certificate of Quality (CQ) from the manufacturer/official distributor upon equipment delivery. Complete registration number or import license as per current regulations. - Operating voltage: 220VAC ±10%, 50/60 Hz (for power adapter charger) / Built-in rechargeable battery. - Operating Environment: ○ Maximum operating temperature ≥ 30ºC (Actual stable operating range from 5ºC to 40ºC) ○ Maximum operating humidity ≥ 70% (Actual stable operating range from 30% to 85%) - Origin: G7 II. Supply Configuration - 01 Main unit (Handle with integrated color LCD display). - 01 Set of reusable curved intubation blades, including at least 3 sizes: - 01 Pediatric size blade (Size 2). - 01 Adult size blade (Size 3). - 01 Blade for difficult airway structures (Size 4). - 01 Rechargeable battery - 01 USB cable set. - 01 Specialized shockproof carrying case. - User manual in English and Vietnamese: 1 set. Body design features: - Compact handheld design, total weight including blade ≤ 380 grams. Color display: - Display area size: ≥ 4.0 inches. - Screen resolution: ≥ 640 x 480 RGB - Aspect ratio: 4:3; Video scan/refresh rate: ≥ 30 FPS. Camera & lens system: - Camera sensor resolution: ≥ 2.0 MP - Optical field of view: ≥ 66°. - Blade tip illumination system: Uses high-brightness LED technology ≥ 800 LUX. Data storage function: - Integrated one-touch photo capture and video recording button on the handle. - Internal data storage capacity: ≥ 4 GB. - Supports USB port connection for data output to a computer or optional connection to an external monitor via a dedicated adapter cable. Power Management & Rechargeable Battery - Rechargeable battery type: Lithium battery or better - Continuous operating time after full charge: ≥ 50 minutes. - Full battery charging time: ≤ 6 hours. IV. Other Requirements - Delivery, installation and user instruction location: Nhan Ai Hospital. - The equipment must be warranted for ≥ 12 months from the date of acceptance and commissioning. - Perform periodic maintenance 4 times/12 months. - Free labor for maintenance (excluding accessory replacement) after the warranty period of ≥ 6 months. - In case of unscheduled inspection or repair, the contractor must be able to respond within: ≤ 48 hours. - Commitment to providing spare parts and consumables for the equipment for a period of ≥ 8 years (circuit components, rechargeable batteries, various blade sizes).

Nhan Ai Hospital, Phu Nghia commune, Dong Nai city

6 CHANNELS ECG MACHINE (6 CHANNELS ECG MACHINE)

2

Female

I. General Requirements - 100% new equipment, manufactured from 2026 onwards - Manufacturer must meet ISO 13485 or ISO 9001 standards - Origin requirements: Provide complete CO, CQ and legal import documents upon delivery. Equipment must meet Class I electrical safety certification, Type CF, with defibrillation protection meeting international medical standards (IEC 60601-1) - Operating voltage: 100V ~ 240V, 50Hz/60Hz - Operating environment: ○ Maximum operating temperature ≥ 30ºC (Stable operating range from 5°C to 40°C) ○ Maximum operating humidity ≥ 70% (Stable operating range from 25% to 95%) - Origin: G7 II. Configuration provided: - 01 Main unit with integrated touchscreen and thermal printer - 01 Standard ECG accessory kit including: - 01 Patient cable (ECG cable). - 04 Limb electrodes (arm/leg clamp electrodes). - 06 Chest electrodes (vacuum suction cups). - 01 Built-in rechargeable battery. - 01 AC power cord. - 01 Thermal printing paper. - 01 Dedicated machine trolley (available for purchase in Vietnam). - User manual in English and Vietnamese: 01 set. III. TECHNICAL SPECIFICATIONS Signal Recording & Acquisition Channels (ECG Input) - Machine type: 6-channel ECG machine. - Number of leads: Simultaneous collection and recording of 12 standard ECG leads. - Technical frequency response range: 0.05 Hz ~ 250 Hz - Signal sampling rate: ≥ 8000 samples/second/channel. - Analog/Digital conversion (A/D Converter): ≥ 24 bits - Heart rate measurement range: Approximately 30 to 300 beats/minute. Noise filtering circuit system - Mechanical/Electromechanical noise filter (EMG Filter): 25/ 35/ 75/ 100/ 150/ 250Hz Color display - Screen type: Touchscreen - Display size: ≥ 7.0 inches (8.0 inches or larger recommended). - Minimum resolution: 800 x 480 pixels. Data storage - Supports USB port or SD card slot for external storage connection. Integrated Thermal Printer Unit - Paper Feed Speed: Full range of selectable settings including 5; 10; 12.5; 25; 50 mm/second. Physical Characteristics & Power Management - Rechargeable Battery Type: Built-in rechargeable battery (Lithium or Ni-MH). - Battery operating time after full charge: ≥ 150 minutes. - Full battery charging time: ≤ 2 hours (Battery reaches 90%). IV. Other Requirements - Delivery, installation and user instruction location: Nhan Ai Hospital. - The equipment must be warranted for ≥ 12 months from the date of acceptance and commissioning. - Perform periodic maintenance 4 times/12 months. - Free labor for maintenance (excluding replacement of accessories) after the warranty period of ≥ 6 months. - In case of unscheduled inspections or repairs, the contractor must be able to respond within ≤ 48 hours. - Commitment to supplying spare parts and consumables for equipment for ≥ 8 years (patient cables, electrode ballasts, thermal recorders, rechargeable batteries).

Nhan Ai Hospital, Phu Nghia commune, Dong Nai city

Digital mobile X-ray machine

1

Female

I. General Requirements - 100% new equipment, manufactured from 2026 onwards - Manufacturer must meet ISO 13485 and CE standards or ISO 13485 and FDA standards - Origin requirements: Complete CO, CQ certificates and legal customs clearance permits. Fully compliant with national technical standards on radiation safety for medical diagnostic X-ray equipment. - Operating voltage: 220VAC ±10%, 50/60 Hz. - Operating environment: ○ Maximum operating temperature ≥ 30ºC (Stable operating range from 10°C to 40°C) ○ Maximum operating humidity ≥ 70% (Stable operating range from 30% to 75%) - Origin: EU II. Configuration provided: - 01 Mobile main unit with integrated heavy-duty wheels, safety emergency braking/stopping system, and power source control cabinet. - 01 High-frequency inverter X-ray source. - 01 X-ray tube (Rotating anode type). - 01 Beam collimator with LED positioning light. - 01 Handheld shutter switch with extension cord. - 01 Wireless digital flatbed sensor. - 01 Digital image acquisition, processing, and control station (using a ≥ 19-inch touchscreen). - 01 Dedicated digital image acquisition, processing, and management software (DICOM 3.0 compatible). - User manuals in English and Vietnamese: 1 set. III. TECHNICAL SPECIFICATIONS Control Cabinet & High-Frequency Generator - Generator type: High-frequency inverter with base-line voltage protection. - X-ray generator power: ≥ 50 kW. - Maximum tube current: 500mA - Shortest exposure time: ≤ 1 millisecond (0.001 sec). - APR (anatomy programs): 400 and can be further configured according to user needs. - Touchscreen display for adjusting technical parameters at the head of the X-ray tube. X-ray Tube - Focal point type: Large focal point ≤ 1.2 mm; Small focal point ≤ 0.6 mm. - Anode Angle: ≥ 14 degrees - Bulb Heat Resistance: ≥ 750 kJ (1060 KHU) ​​- Anode Heat Resistance: ≥ 210 kJ (300 KHU) ​​- Bulb Heat Dissipation Rate: ≥ 150W (13 KHU/min ~ 217 HU/sec) - Anode Heat Dissipation Rate: ≥ 870W (1226 HU/sec) Beam Collimator - Maximum collimator field at SID distance = 100 cm - Field Positioning Light System: Uses high-brightness LED technology ≥ 160 lux. - Positioning Utility: Integrated automatic light shut-off after a waiting period (e.g., automatically shuts off after 30 seconds). - Mechanical Capability: Allows flexible rotation of the Collimator assembly to position the imaging area. Wireless Flat Panel Sensor (Wireless FPD) - a-Si TFT technology, high-grade Cesium Iodide (CsI) light-emitting material, optimized for reducing radiation dose to patients. - Pixel size: ≤ 140 micrometers - Spatial resolution: 3.3-3.5 lp/mm - Resolution: ≥ 3072 x 3072 pixels - Image size: ≥ 430 mm x 430 mm - Grayscale: 16 bits - Image acquisition time: 3 seconds - Maximum load: 200 kg per pixel with a diameter of 40 mm; 400 kg for the entire panel - Automatic storage capacity: ≥ 200 images - Dust and water resistance standard: IP67 or higher - Battery life: ≥ 7 hours (single battery) in operating mode and 8 hours in standby mode; ≥ 15 hours (dual battery) in operating mode and 16 hours in standby mode. - X-ray emission detection: Automatic Exposure Detection (AED) function does not require hardware connection to the X-ray cabinet. 153:158+156:156 - Transmission: High-speed Wi-Fi wireless connection (IEEE 802.11a/b/g/n/ac or equivalent). Image processing station (Workstation) - Workstation hardware: Equipped with a minimum Intel Core i5 processor (or equivalent), RAM capacity ≥ 4 GB (16 GB recommended), high-speed SSD data storage ≥ 128 GB (512 GB recommended). High-resolution, sharp image display with touch screen support. - Software processing tools: Full suite of algorithmic tools for image quality enhancement, noise smoothing, and clinical geometric measurement tools (distance measurement, angle measurement, zoom, cropping, image flipping, inserting text/notes in L/R direction). Supports output of common image formats (JPEG, TIFF, BMP). Mobile mechanical structure: - Equipped with a motor for assisted movement. - Equipped with proximity sensors on the front bumper to prevent collisions. IV. Other requirements - Delivery, installation, and user training location: Nhan Ai Hospital. - The equipment must have a warranty of ≥ 12 months from the date of acceptance and commissioning. - Perform periodic maintenance 4 times/12 months. - Free labor for maintenance (excluding replacement of accessories) after the warranty period of ≥ 6 months. - The device can connect to hospital management software via HIS/LIS/PACS connections: The system software must be fully integrated and compatible with the international medical standard DICOM 3.0. It must fully support functional connection modules including: DICOM Modality Worklist (automatically receives patient assignment lists from the hospital information system HIS/RIS), DICOM Storage (pushes digital images to the hospital's PACS storage system), and DICOM Print (connects to medical film printers). - In case of unscheduled inspections or repairs, the contractor must be able to respond within 48 hours. - Commitment to providing spare parts and consumables for the equipment for ≥ 8 years (X-ray tube, FPD sensor plate, rechargeable battery, power supply microchips).

Nhan Ai Hospital, Phu Nghia commune, Dong Nai city

VEIN SCREEN MACHINE (VEIN SCREEN MACHINE)

1

Female

I. General Requirements - 100% new equipment, manufactured from 2026 onwards. - The manufacturer must meet ISO 13485 or CE quality management standards. - Origin requirements: Complete CO and CQ documents upon delivery. - Operating voltage: 220VAC ±10%, 50/60 Hz (for common adapter chargers) / Built-in rechargeable Lithium battery (standard USB charging output voltage 5V / 2.0A). - Operating environment: ○ Maximum operating temperature ≥ 30ºC (Stable operating range from 5°C to 40°C) ○ Maximum operating humidity ≥ 70% (Stable operating range from 30% to 85%) II. Supply Configuration - 01 Compact handheld venography main unit (with built-in rechargeable battery). - 1 set of power cord and power adapter. - 1 device calibration card. - 1 shockproof protective case/suitcase (made of aluminum or equivalent material). - 1 medical tourniquet included with the device. - User manual in English and Vietnamese: 1 set. III. TECHNICAL SPECIFICATIONS Projection & Optics Technology - Infrared wavelength: Reaches the range of 760 nm to 940 nm. - Subcutaneous blood vessel detection depth: Approximately 0 to 10 mm. - Optimal projection positioning distance: Approximately 15 cm to 20 cm. - Accuracy of displayed blood vessel position: Amplitude error ≤ ± 0.3 mm. - Blood vessel size recognition capability: Clearly identifies veins with a diameter greater than or equal to ≥ 1 mm. Image Optimization Mode - Customizable Color Display: Integrates a variety of different color modes (Minimum 7 colors, recommended 12 colors) compatible with various skin tones and clinic lighting conditions. - Customizable Projection Area Size: Supports flexible customization of 3 different projection area sizes (Large, Medium, Small) compatible with adults, children, and infants. - Brightness Adjustment: Supports customizable configuration of at least 4 different brightness levels (recommended 6 levels). - Inverse Mode: Features background inversion to reduce interference from hair and skin texture, making blood vessels more visible and intuitive. - Enhance Mode: Enhances image sharpness/resolution to locate small or deeply embedded veins. Data Storage Function - Image Storage Function: Supports capturing and storing vein images directly in the device's memory for clinical monitoring and analysis. - Built-in Memory Storage Capacity: Stores a minimum of 4000 image sets (6000 sets recommended). - Data Output Capability: Designed with a dedicated communication port for connecting to a computer to access, back up, and manage image data. Power Management & Operation System - Smart Sleep Mode: Automatically switches to a low power consumption state when not in continuous use (allows setting sleep time) to protect the battery. - Automatic Shutdown Feature: Automatically shuts off completely when the device is inactive for a certain period of time. - Battery Monitoring System: Displays battery capacity visually on the projection interface. Audible or flashing light alerts indicate low battery. - System operating noise ≤ 35 dB. Power supply specifications: - Integrated battery type: Rechargeable Lithium battery with multiple recharge cycles and long lifespan. - Battery pack capacity: ≥ 3000 mAh. - Continuous operating time after a full charge ≥ 3 hours. IV. Other requirements: - Delivery, installation, and user instruction location: Nhan Ai Hospital. - The equipment must be warranted for ≥ 12 months from the date of acceptance and commissioning. - Perform periodic maintenance 4 times/12 months. - Free labor for maintenance (excluding replacement of accessories) after the warranty period ≥ 6 months. - In case of unscheduled inspection or repair, the contractor must be able to respond within: ≤ 48 hours. - Commitment to providing spare parts and consumables for the equipment for a period of ≥ 8 years (Medical rechargeable battery pack, power adapter, aluminum protective case).

Nhan Ai Hospital, Phu Nghia commune, Dong Nai city