Medical equipment quotation

ELECTRICAL EEG

1

Female

I. GENERAL REQUIREMENTS - Year of manufacture: 2026 onwards, 100% new - Complies with standard: ISO 13485 - Power supply: 220V ± 10%; 50-60Hz - Operating environment: + The device must be able to operate within a temperature range of ≤ 15 to ≥ 30°C. + The device must be able to operate within a humidity range of ≤ 35 to ≥ 75%. II. CONFIGURATION REQUIREMENTS - Main unit: 1 unit - Tripod: 1 unit - Light stimulator: 1 set - EEG disc electrodes with cable: 1 set - Sphere electrodes: 3 units - EEG ear electrodes: 3 units - EEG electrode caps: 3 units - Software: 1 set - Computer and monitor: 1 set - Accessories: keyboard, mouse, connecting cables…: 1 set - Black and white printer: 1 set - Uninterruptible Power Supply (UPS): 1 set III. TECHNICAL REQUIREMENTS 1/ EEG Channel/ EP Channel: (Electroencephalogram/Emission Voltage Recording Channel) - Number of channels: ≥ 21 channels - Sampling rate range: From ≤ 100 to ≥ 5000 Hz (Minimum ≥ 6 steps) - Input voltage range: From 1 to ≥ 12000 µV. - Voltage measurement error: + Range from 10 to 50 µV: ≤ ± 15% + Range from 51 to 12000 µV: ≤ ± 5% + Intermittent measurement error within 10 µs to 10s: ≤ ± 2% - Signal acquisition sensitivity: From 1 to ≥ 1000 µV/mm (Minimum ≥ 10 steps) - Sensitivity error: ≤ ± 5% - Adjustable scanning speed for EEG recording: From ≤ 5 to ≥ 900 mm/second; Adjustment step ≤ 1 mm/second. - Scanning speed error: ≤ ± 2% - High-pass filter: From ≤ 0.1 to ≥ 10 Hz; Adjustment step ≤ 0.01Hz - Low-pass filter: From ≤ 8 to ≥ 200 Hz; Adjustment step ≤ 0.1Hz - Input noise level in the range: From ≤ 0.5 to ≥ 200Hz: ≤ 0.3 µV - Input impedance: ≥ 100MΩ - Patient leakage current: ≤ 80nA 2/ Multi-purpose channel: (EOG, EMG…) - Number of channels: ≥ 4 channels - Input voltage range: From ≤ 0.5 to ≥ 100mV - Voltage measurement error: + From 200µV to 500µV: ≤ ± 15% + From 0.5mV to 100mV: ≤ ± 7% - Sensitivity: From 0.001 to ≥ 0.5 mV/mm (Minimum ≥ 10 steps) - High-pass filter: From ≤ 0.05 to ≥ 10 Hz (Minimum ≥ 8 steps) - Low-pass filter: From ≤ 5 to ≥ 200 Hz (Minimum ≥ 8 steps) - Input noise level in the range from ≤ 0.05 to ≥ 200Hz: ≤ 3 µV - Input impedance: ≥ 100 MΩ - Patient leakage current: ≤ 80 nA 3/ Light stimulator - Number of channels: ≥ 1 channel - Stimulation duration: From 0.1 to ≥ 2800 ms - Relative deviation of stimulation duration: ≤ ±10% - Uses LED technology - Maximum lamp brightness: ≥ 950 cd/m2 - Stimulation frequency: From 0.1 to ≥ 100 Hz - Relative deviation of stimulation frequency: ≤ ±1% - Capable of stimulating the left, right, and both sides - Software must have at least the following features: + Recording and analyzing electroencephalogram (EEG) signals + Automatic detection of spikes and peaks + Creating and editing EEG leads + Video EEG monitoring + Automatic EEG report generation + Brain mapping and bar graphs of EEG analysis results + Discharge mapping + Ability to read results 4/ Computer and printer 4/1/ Computer: - Operating system: Windows 10 or equivalent - Processor: Core i5 or higher - Processing speed ≥ 1.90 GHz - RAM: ≥ 8GB - Hard drive: ≥ 1 TB - USB connection ports 4/2/ Monitor: - Type: LCD monitor - Size ≥ 17 inches - Resolution: ≥ (1152 x 864) pixels 4/3/ Printer: - Windows compatible. - Black and white laser printer. - Paper size: A4/A5. - Minimum printing speed: ≥ 18 pages/minute. 5/ UPS: - Online UPS - Power: ≥ 2KVA 6/ The machine has LIS/HIS network connectivity IV. OTHER REQUIREMENTS - Warranty period ≥ 12 months. - Delivery time: ≤ 90 days at the user's location. - Installation and testing immediately after handover, performed by qualified and experienced engineers. - Personnel training: on installation, testing, operation, and maintenance of equipment until proficiency is achieved. - In case of any malfunction, technical staff will be on-site within 48 hours to resolve the issue. - Commitment to providing consumables and spare parts for 8 years. - Provision of user manuals in English and Vietnamese. Service manual in English. - Commitment to providing all necessary quality certificates (CQ) and certificates of origin (CO) for the goods. - Provision of customs import declarations upon delivery for imported equipment. - The contractor is responsible for inspecting the equipment and completing the necessary documentation for licensing and commissioning for equipment requiring permits from relevant authorities. - Provision of sales licenses, sales authorizations from the manufacturer or distributor, partnership certificates, technical support and warranty commitments from the manufacturer or distributor, or other equivalent documents. - Provision of a periodic maintenance plan during the warranty period as stipulated by the manufacturer. - Provide a quotation for comprehensive maintenance and servicing after the warranty period. - Request a quotation for consumables and replacement parts. - Guarantee that the goods comply with legal regulations according to Decree 98/2021/ND-CP and other relevant legal documents (if any).

A Luoi Medical Center Address: Village 6, A Luoi 2 Commune, Hue City

High frequency electric scalpel

1

Female

I. GENERAL REQUIREMENTS - Year of manufacture: 2026 onwards, 100% new - Complies with standard: ISO 13485 - Power supply: 220V ± 10%; 50-60Hz - Operating environment: + The device must be able to operate within a temperature range of ≤ 15 to ≥ 30°C. + The device must be able to operate within a humidity range of ≤ 35 to ≥ 75%. II. CONFIGURATION REQUIREMENTS The main unit and standard accessories include: - Main unit: 1 unit - Reusable, sterilizable handpieces: 3 units - Disposable neutral electrodes: 5 units - Neutral electrode cable: 1 unit - Bipolar electrode: 1 unit - Foot pedal: 2 units - Thin electrode tips (approx. 7cm): 3 units - Thin electrode tips (approx. 16cm): 3 units - Metal electrode tips (approx. 7cm): 3 units - Round electrode tips (approx. 6cm): 3 units - Power cord: 1 unit III. TECHNICAL REQUIREMENTS - The device is designed for use in operating rooms, procedure rooms, etc. - It has a warning function and displays error codes during operation. - It has a continuous current leakage monitoring function. - Monopolar operating frequency: ≥ 400 KHz - Bipolar operating frequency: ≥ 500 KHz - Monopolar cutting mode: + Maximum power ≥ 250 W + Impedance approximately: 300 Ω - 80% cutting mode in monopolar cutting/cauterization program: + Maximum power ≥ 200 W + Impedance approximately: 300 Ω - 60% cutting mode in monopolar cutting/cauterization program: + Maximum power ≥ 150 W + Impedance approximately: 300 Ω - 40% cutting mode in monopolar cutting/cauterization program: + Maximum power ≥ 100 W + Approximate impedance: 300 Ω - Mixed cutting-cauterization mode: + Maximum power ≥ 200 W + Approximate impedance: 300 Ω - Bipolar cutting mode: + Maximum power ≥ 100 W + Approximate impedance: 50 Ω. - 80% cutting mode in bipolar cutting-cauterization program: + Maximum power ≥ 100 W. + Approximate impedance: 50 Ω. - 60% cutting mode in bipolar cutting-cauterization program: + Maximum power ≥ 100 W + Approximate impedance: 50 Ω. - 40% cutting mode in bipolar cutting-cauterization program: + Maximum power ≥ 80 W + Approximate impedance: 50 Ω - Bipolar cauterization mode: + Maximum power ≥ 100 W + Approximate impedance: 50 Ω. - Bipolar hemostasis mode: + Maximum power ≥ 120 W + Impedance approximately: 50 Ω. IV. OTHER REQUIREMENTS - Warranty period ≥ 12 months. - Delivery time: ≤ 90 days at the user's location. - Installation and commissioning immediately after handover, performed by qualified and experienced engineers. - Personnel training: on installation, commissioning, operation, and maintenance of equipment until proficiency is achieved. - In case of a malfunction, technical staff will be on-site within 48 hours to resolve the issue. - Commitment to providing consumables and spare parts for 8 years. - Provision of user manuals in English and Vietnamese. Service manual in English. - Commitment to providing all necessary quality certificates (CQ) and certificates of origin (CO) for the goods. - A customs import declaration is required upon delivery of imported equipment. - The contractor is responsible for inspecting the equipment and completing the necessary documentation for licensing and commissioning as required by the relevant authorities. - A sales license, sales authorization from the manufacturer or distributor, a partnership certificate, a technical support and warranty commitment from the manufacturer or distributor, or other equivalent documentation is required. - A periodic maintenance plan is in place during the warranty period as stipulated by the manufacturer. - A comprehensive maintenance and repair quotation is provided after the warranty period. - A quotation for consumables and spare parts is required. - The contractor commits to ensuring that the goods comply with legal regulations under Decree 98/2021/ND-CP and other relevant legal documents (if any).

A Luoi Medical Center Address: Village 6, A Luoi 2 Commune, Hue City

Electrocardiogram

1

Female

I. GENERAL REQUIREMENTS - Year of manufacture: 2026 or later, 100% new - Meets standard: ISO 13485 - Power supply: 220V ± 10%; 50-60Hz - Operating environment: + The device must be able to operate in a temperature range of ≤ 15 to ≥ 30°C. + The device must be able to operate in a humidity range of ≤ 35 to ≥ 75%. II. CONFIGURATION REQUIREMENTS - Main unit: 1 unit. - ECG cable: 1 unit. - Limb electrode clamp set: 1 set - Chest electrode set: 1 set - Rechargeable battery: 1 unit - Thermal printing paper: 1 roll - Thermal printer: 1 unit - Power cord: 1 unit III. TECHNICAL REQUIREMENTS - Basic examination capability: Heart rate, RR, PR, QRS, QT interval, QTcB, QTcF, electrical axis, SV1, RV5 (6) - Number of measurement channels: ≥ 3 channels - Display screen: + Screen type: Color LCD, touch screen + Size: ≥ 6 inches + Resolution: ≥ (800 x 480) dots - Heart rate measurement range: From ≤ 40 to ≥ 300 bpm - Heart rate measurement range accuracy: ≤ ± 2 bpm - Standard sensitivity: ≤ 10mm/Mv - Sensitivity can be selected manually or automatically. - Minimum sensitivity levels: ¼, ½, 1, 2 - Input impedance: ≥ 2 MΩ - Recovery time: ≤ 5 seconds - Frequency response: From ≤ 0.1Hz to ≥ 150Hz - Sampling rate: ≥ 6000 samples/second - Leads: 12 standard leads - Internal noise: ≤ 40Mv - A/D converter: ≥ 18-bit - Storage capacity: ≥ 500 ECG data - Printer: + Thermal printer type + Selectable printing speed: 5, 10, 12.5, 25, 50 mm/s + Printing density: * Amplitude: 8 dots/mm * Time axis: 40 dots/mm - Number of printing channels: Selectable 1 or 3 channels - Battery type: + Battery type: Ni-MH or equivalent + Continuous operation capability: ≥ 120 minutes - Peripheral connection ports: LAN port, USB IV. OTHER REQUIREMENTS - Warranty period ≥ 12 months. - Delivery time: ≤ 90 days at the user's location. - Installation and commissioning immediately after handover, performed by qualified and experienced engineers. - Personnel training: on installation, commissioning, operation, and maintenance of equipment until proficiency is achieved. - In case of a malfunction, technical staff will be on-site within 48 hours to resolve the issue. - Commitment to providing consumables and spare parts for 8 years. - Provision of user manuals in English and Vietnamese. Service manual in English. - Commitment to providing all necessary quality certificates (CQ) and certificates of origin (CO) for the goods. - A customs import declaration is required upon delivery of imported equipment. - The contractor is responsible for inspecting the equipment and completing the necessary documentation for licensing and commissioning as required by the relevant authorities. - A sales license, sales authorization from the manufacturer or distributor, a partnership certificate, a technical support and warranty commitment from the manufacturer or distributor, or other equivalent documentation is required. - A periodic maintenance plan is in place during the warranty period as stipulated by the manufacturer. - A comprehensive maintenance and repair quotation is provided after the warranty period. - A quotation for consumables and spare parts is required. - The contractor commits to ensuring that the goods comply with legal regulations under Decree 98/2021/ND-CP and other relevant legal documents (if any).

A Luoi Medical Center Address: Village 6, A Luoi 2 Commune, Hue City

Echocardiography probe

1

Female

I. GENERAL REQUIREMENTS - Year of manufacture: 2026 and later, 100% new II. CONFIGURATION REQUIREMENTS - Sector probe: 01 piece III. TECHNICAL REQUIREMENTS Sector type ultrasound probe has features that ensure compatibility with existing ultrasound machines being used at the Center, Model: LOGIQ F8 manufactured by GE Healthcare. At the same time, it meets the following technical requirements: - Examination applications: Cardiac, transcranial - Has biopsy guidance function - Frequency range: From ≤ 1.7 to ≥ 4 MHz - Number of concussions: ≥ 64 - Field of view (FOV): ≥ 120° - B-Mode image frequency: Has at least ≥ 3 frequencies (2.0, 3.0, 4.0 MHz) - Harmonic imaging frequency: At least ≥ 4 frequencies (3.0, 3.2, 3.5, 4.0 MHz) - Color flow Doppler frequency/ Power Doppler/ Pulsed Doppler (CFM/PDI/PWD): At least ≥ 4 frequencies (1.7, 2.0, 2.5, 3.3 MHz) - Continuous Doppler frequency (CWD): ≥ 1.9 MHz IV. OTHER REQUIREMENTS - Warranty period ≥ 06 months. - Delivery time: ≤ 90 days at the user unit. - Installation and test run immediately after handover, performed by qualified and experienced engineers. - Personnel training: on installation, commissioning, operation, and maintenance of equipment until proficiency. - When a problem occurs, technical staff will be present within 48 hours to resolve it. - Commitment to providing full certificates of quality (CQ) and origin (CO) of the goods. - Have a customs import declaration upon delivery for imported equipment - Have a sales license, sales authorization letter from the manufacturer or distribution agent, or a partnership certificate or commitment to technical support, warranty from the manufacturer or distribution agent, or other documents of equivalent value. - Have a periodic maintenance plan during the warranty period according to the manufacturer's regulations. - Commitment that the goods meet legal regulations according to Decree 98/2021/ND-CP and relevant legal documents (if any).

A Luoi Medical Center Address: Village 6, A Luoi 2 Commune, Hue City