Dong Runze GIGA Mobile P2 PRC CT Lab Clinics Medical Truck
Product Description
Dong Runze GIGA Mobile P2 Laboratory Clinics Medical Truck
Main Technical Parameters
Item | Details |
Overall Dimensions (mm) | 11950×2530×3810 |
Gross Mass (Kg) | 18000 |
Curb Mass (Kg) | 17500 |
Rated Load Mass (Kg) | 305 |
Front-row Passengers (Person) | 3 |
Anti-lock Braking System (ABS) | Yes |
Approach Angle/Departure Angle (°) | 15/14 |
Front Overhang/Rear Overhang (mm) | 1335/3415 |
Axle Load (Kg) | 6500/11500 |
Wheelbase (mm) | 7200 |
Number of Axles | 2 |
Maximum Speed (km/h) | 89 |
Number of Leaf Springs | 7/7+7 |
Number of Tires (Piece) | 6 |
Tire Specification | 295/80R22.5 16PR, 295/80R22.5 18PR |
Front Track (mm) | 1960, 1990, 2030 |
Rear Track (mm) | 1855 |
Steering Type | Steering Wheel |
VIN (Vehicle Identification Number) | LWLYUAJK××××××××× |
Engine Parameters
Engine Model | Engine Manufacturer | Displacement (ml) | Power (kw)/Horsepower (ps) |
4HK1-TCG60 | Isuzu (China) Engine Co., Ltd. | 5193 | 151/205 |
Vehicle Fuel Parameters
SPV vehicle Optional equipped with workbenches, CT, X-ray machines and other medical equipment. It can be optionally equipped with medical-specific facilities such as different models of CT medical lighting lamps and ultraviolet disinfection lamps, mainly used for medical examinations, etc. Optional equipment includes: biosafety cabinet; mobile laboratory analysis equipment; hydraulic sterilization equipment; power supply system; water supply and drainage system for medical testing; and electric rotating steps. Air conditioning and side styles are also optional.
The left and right side protections are skirt structures, and the rear protection is a skirt structure with a ground clearance of 500mm.
Truck mounted Nucleic Acid Testing Vehicle Technical Specifications
2. Basic Requirements for Truck-type Nucleic Acid Testing Vehicles
2.1 The experimental area in the mobile nucleic acid testing vehicle shall include a reagent preparation area, a sample preparation area, an amplification detection and analysis area, and a cleaning and disinfection area. The three main experimental areas shall be equipped with independent buffer rooms, and the entire experimental area shall meet the standards of a biosafety level 2 laboratory. The testing vehicle shall mainly consist of a chassis, a side box, a compartment, a fresh air purification air conditioner, a negative pressure system, an electrical control system, an alarm system, a door interlock system, a monitoring system, a wastewater treatment system, a waste gas treatment system, disinfection facilities, experimental tables, water tanks, eyewash stations, etc.
2.2 Overall external dimensions (length × width × height) of the vehicle: ≥11950×2500×3800mm;
2.3 External dimensions (length × width × height) of the medical compartment (laboratory): ≥9700×2500×2700mm
2.4 The modified whole vehicle shall meet the local licensing standards. Provide a screenshot of the announcement parameters of the whole vehicle and the announcement inquiry website, and the announcement type shall be applicable to special vehicles rather than ordinary or freight vehicles;
2.5 The whole vehicle shall include vehicle purchase tax and three-year vehicle insurance premium.
3. Technical Indicator Requirements for Truck-type Nucleic Acid Testing Vehicles
3.1 Technical Parameters of the Chassis of the Testing Medical Vehicle
3.1.1 The chassis shall be a Class II cargo chassis.
3.1.2 Overall external dimensions (length, width, height) of the vehicle: ≥11950×2500×3800mm
3.1.3 Curb weight (kg): ≥6100
3.1.4 Number of passengers allowed in the cab: 3
3.1.5 Axle load (kg): ≥16500/11500
3.1.6 Approach angle/departure angle (°): ≥115/14
3.1.7 Front overhang/rear overhang (mm): ≥1300/3100
3.1.8 Engine power: ≥150kW
3.1.9 Equipped with ABS anti-lock braking system
3.1.10 Transmission: Manual or automatic
3.1.11 Wheelbase (mm): ≤7200
3.1.12 Tire specification: 295/80R22.5 16PR or 295/80R22.5 18PR
3.1.13 Number of leaf springs: 7/7+7
3.1.14 Fuel type: Diesel
3.1.15 Emission standard: GB17691-2018 National VI
3.1.16 Front track (mm): ≥1900, Rear track (mm): ≥1800
3.1.17 Spring shock-absorbing seats, power windows
3.1.18 Air brake, power steering
3.1.19 LCD display, reversing image, central door lock
3.2 Modified Technical Parameter Requirements
3.2.1 The mobile P2 laboratory compartment (length × width × height) shall be ≥9700×2500×2700mm, divided into a buffer corridor (≥4.2M⊃2;), a reagent preparation area (≥2.6M⊃2;), a sample preparation area (≥5.8M⊃2;), an amplification area (≥3.5M⊃2;), and a cleaning and disinfection room (≥2.7M⊃2;). Each area shall be independent and not directly connected. Each independent experimental area shall be equipped with a special buffer room (≥0.7M⊃2;) for staff to change work clothes and shoes.
3.2.2 External Structure of the Compartment
[3.2.2.1] Adopt 20mm polyurethane composite board bonded and riveted to ensure the flatness of the large surface and achieve the effect of sealing and thermal insulation for all-weather use. Provide a test report issued by a third-party testing institution entrusted by the manufacturer and physical pictures.
[3.2.2.2] Equip with a set of hydraulic balancing system (≥8T) with automatic leveling and one-key automatic balancing functions. Provide physical pictures and technical indicator descriptions of the hydraulic balancing support system sealed with the manufacturer's official seal.
[3.2.2.3] Install a clean water tank, a sewage tank, wastewater and waste gas treatment devices, and an air conditioning unit in the luggage compartment. Provide physical pictures.
3.2.3 Internal Structure of the Compartment
[3.2.3.1] Steel frame structure. The four corners shall use high-quality 400x50x4 rectangular tubes as the main support of the frame, and the rest of the frame shall be assembled with 60x40x3 and 40x40x2.5 rectangular tubes to ensure the strength and safety of the compartment;
[3.2.3.2] The main beam of the compartment underframe shall use 140x70×6 channel steel as the longitudinal beam, and the cross beam shall be welded with 60x40x3 rectangular tubes. The underframe and the chassis frame shall be connected with 10 φ18 U-bolts to ensure that the compartment and the chassis are integrated and will not move during the operation of the vehicle.
3.2.4 Experimental Tables and Cabinets
[3.2.4.1] Adopt laboratory-specific antibacterial 12.7mm solid chemical-resistant panel with strong corrosion resistance and antibacterial ability;
[3.2.4.2] The cabinet body shall be made of 1.2mm galvanized steel sheet. The surface shall be degreased, washed with water, pickled, washed with water, neutralized, phosphated, washed with water, high-pressure rinsed, dried, and then sprayed with epoxy resin powder for high-temperature curing. The coating thickness shall be greater than 75 μm, with strong corrosion resistance and antibacterial ability.
3.2.5 Wastewater Treatment System
[3.2.5.1] Daily treatment capacity of laboratory comprehensive wastewater: ≥500L/D;
[3.2.5.2] Equipment power supply: AC220V, total power not exceeding 4.5kw;
[3.2.5.3] The equipment shall be made of high-quality corrosion-resistant materials without leakage, and no civil engineering tank is required; PE lining + external electrostatic electrophoresis carbon steel spray coating, corrosion-resistant and durable;
[3.2.5.4] The wastewater treated by the equipment shall meet the requirements of the national medical institution wastewater discharge standard GB18466-2005 and the CJ343-2010 standard for wastewater discharge into urban sewers.
3.2.6 Waste Gas Treatment System
[3.2.6.1] Treatment capacity of laboratory comprehensive waste gas: ≥2500M⊃3;/H;
[3.2.6.2] Equipment power supply: AC220V, total power not exceeding 3.5kw;
[3.2.6.3] The equipment shall adopt spray coating process, and the plate thickness shall be ≤1.5MM;
[3.2.6.4] The waste gas treated by the equipment shall meet the national medical institution waste gas discharge standard, with dust content below 10MG/L and no toxic components.
4. Equipment Technical Indicator Requirements
4.1 2 High-throughput Nucleic Acid Extraction Systems
1. Methodology: Magnetic bead method
2. Maximum throughput: ≥96 samples/time
3. Sample types: Whole blood, serum, plasma, throat swab, secretion, exfoliated cells, urine, sputum, feces, FFPE tissue, animal and plant tissue, dried blood spot, saliva, lung lavage fluid, etc.
4. Magnetic rod sleeve handling mode: Automatic picking and placing of magnetic rod sleeves without manual operation
5. Extraction inter-hole difference: CV≤3%
6. Anti-cross-contamination: Ultraviolet disinfection module, ventilation facilities, aerosol high-efficiency filter, negative pressure exhaust function
7. Intelligent program: Intelligent ultraviolet lamp disinfection and automatic shutdown
8. Power failure protection: After unexpected power failure and power recovery, the experiment can be selected to continue running
9. Power-on self-test: Automatic initialization and temperature control self-test after power-on
10. Chamber door protection: If the chamber door is opened by mistake, the program pauses, and continues running after closing the chamber door
11. Program management: Create, edit and delete mode programs
12. The manufacturer shall provide the first-class medical device registration certificate and first-class medical device production registration certificate of the product;
4.2 4 Fluorescent Quantitative PCR Instruments
13. Detection throughput: ≥96
14. Applicable consumables: 0.2mL 96-well plates, 8-tube strips and single tubes (applicable to consumables of different colors)
15. ★ Number of fluorescence channels: ≥4
16. Applicable dyes/probes: Channel 1: FAM, SYBR Green I; Channel 2: VIC, HEX; Channel 3: ROX, Texas Red; Channel 4: Cy5
17. Reaction system: 5~100uL
18. Linear range: 1~10⊃1;⁰ copies
19. Operation mode: Touch screen control for equipment operation; PC direct connection
20. Automatic sample chamber: Electric chamber door, no need to manually touch the sample chamber, reducing the risk of contamination
21. Power failure protection: Memory function after power failure, and can continue running the unfinished experiment from the power failure step when power is restored.
22. Storage: ≥1000 experimental data files
23. Light source: High-brightness, long-life and maintenance-free LED light source
24. Temperature uniformity: ≤±0.25℃
25. Temperature accuracy: ≤±0.15℃
26. Analysis functions: Qualitative analysis, absolute quantitative analysis, relative quantitative analysis, key fluorescence analysis, melting curve analysis, SNP analysis, etc.
27. The manufacturer shall provide the first-class medical device registration certificate and first-class medical device production registration certificate of the product;
4.3 Nucleic Acid Rapid Detection System
28. ★ Sample capacity: 16×0.2ml centrifuge tubes (5-100 μl), compatible with conventional 0.2ml 8-tube strips and single tubes
29. Reaction sensitivity: 10-10⊃1;⁰ Copies
30. Fluorescent dyes: F1: FAM, SYBR Green Ⅰ; F2: HEX, VIC, JOE, TET, YELLOW; F3: ROX; F4: CY5
31. Number of channels: ≥4 channels
32. Optical system: High-brightness LED scanning, photoelectric sensor scanning detection, no calibration required
33. Detection reagents: Open detection reagent consumables (general for conventional PCR projects)
34. Uniformity: ≤±0.2℃
35. Temperature control accuracy: ≤±0.1℃
36. Software: The instrument can directly perform result and data analysis, and is equipped with special computer-based analysis software
37. Registration certification: With national medical device registration certificate
4.4 2 Sets of Manual Single-channel Pipettes
38. The lower part of the pipette can be cleaned and disinfected.
39. Digital display mode: Digital display window, clear and easy to read.
40. Tip removal function: Independent tip ejection system to avoid misoperation and hand fatigue.
41. Single-channel volume range: 0.5-10ul; 2-20ul; 10-100ul; 100-1000ul;
42. Each pipette is provided with a calibration certificate at the factory.
43. Chemical corrosion resistance and UV resistance.
4.5 1 Electric 8-channel Pipette
44. Has 8 main modes and 6 additional functions including pipetting, reverse pipetting, manual pipetting, multi-dispensing, dilution, sequential dispensing, multi-aspiration and titration.
45. Tip removal function: Electric tip ejection, compatible with tips of other brands.
46. Calibration adjustment can be performed for liquids of different densities.
47. Two charging modes: Direct charging with AC adapter (can be charged via USB interface) or charging with charging stand.
48. The lower part can be autoclaved
49. Volume range: 30-300 μl
4.6 2 Units of -20℃ & 4℃ Low-temperature Refrigerators
50. Refrigeration temperature adjustable from 2~8℃, freezing temperature adjustable from -20~-30℃, and the refrigeration compartment can be used independently.
51. Effective volume ≥280L, refrigeration volume ≥180L, product height ≤1850mm,
52. Two alarm modes (sound buzzer alarm, flashing alarm), over-temperature alarm, sensor failure alarm, power failure alarm, refrigeration compartment door opening alarm, remote alarm.
53. Equipped with independent door lock buckles, which can be equipped with double padlocks.
54. With 2 test holes, optional USB interface, which can automatically save the temperature data in the box for ten years.
55. With medical device registration certificate, and the bid model name must be consistent with the registration certificate.
4.7 1 Constant Temperature Water Bath
56. Touch-type PID temperature control system with high temperature control accuracy, stable and reliable performance
57. Thickened stainless steel inner tank with thermal insulation layer
58. Temperature fluctuation: ≤0.3℃
59. Inner tank size: ≥600×300×210mm
60. Heating power: ≥1500W
4.8 3 Mini Centrifuges
61. Maximum speed: ≥5000rpm
62. Rotor capacity: 8 x 0.2/0.5/1.5/2.0ml centrifugation; 16 x 0.2ml PCR tubes; 2 x 0.2ml PCR 8-tube strips
63. Operation time: Continuous operation
4.9 2 Vortex Oscillators
64. Oscillation mode: Circular
65. Speed range: 100-2700rpm
66. Operation mode: Continuous operation / spot operation
67. Shell protection level: IP21
4.10 1 96-well Plate Centrifuge
68. Maximum speed: ≥2500rpm/min
69. Capacity: 2X96-well PCR plates
70. Maximum relative centrifugal force: ≥500xg
71. Rotor: Vertically fixed
4.11 1 96-well Microplate Mixer
72. DC brushless motor, quiet operation and maintenance-free
73. Continuous working function
74. Speed range: 0-1500rpm
75. Protection level: IP21
76. Operation mode: Circular
4.12 Biosafety Centrifuge
77. Can centrifuge 3ml and 5ml centrifuge tubes
78. Speed: ≥4000 revolutions per minute
4.13 1 Barcode Printer
79. Printing technology: Thermal transfer/thermal
80. Printing resolution: ≥300dpi
81. Maximum printing speed: ≥101.6mm/s
82. Label size range: 20-118mm;
83. Communication interface: Serial port/USB/internal Ethernet/USB Host
4.14 1 Barcode Scanner
84. Optical resolution: 640×480dpi
85. Scanning angle: Supports 360-degree rotation, 45-degree elevation angle, 65-degree tilt angle scanning
86. Interface: RS232/USB keyboard emulation/USB serial port emulation
87. Number of barcodes decoded per scan: 1 barcode
88. Connection to information system: Supported
4.15 1 Office Laptop
89. Processor: ≥ i3
90. ≥14-inch full HD LCD screen
91. Memory ≥4G
92. ≥1T mechanical hard disk
93. System: Windows10, supporting Windows7 system
94. Must be an energy-saving product, providing government procurement energy-saving product certification certificate.
4.16 1 Autoclave
95. Volume ≥50L
96. Rated working temperature ≥134℃
97. The sterilization chamber and sterilization basket are made of high-quality stainless steel SUS304 material with internal polishing treatment.
98. Flip-type quick-opening door structure, equipped with door safety interlock device and door detection device. The door cannot be opened when there is pressure, and the program cannot run if the door is not closed properly.
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