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Dong Runze GIGA Mobile P2 PRC CT Lab Clinics Medical Truck

Dong Runze GIGA Mobile P2 PRC CT Lab Clinics Medical Truck
4HK1-TCG60 Isuzu (China) Engine
Optional workbenches, CT, X-ray machines and other medical equipment
Price for refer only. Final Price Offer Discount.
Price: $ 445000
Availability:
Quantity:

  • DRZ5180XYL03XHA

  • DRZ

  • 870590400

Dong Runze GIGA Mobile P2 Laboratory Clinics Medical Truck

DRZ GIGA Mobile PRC Laboratory Clinics Medical Trucks (6)GIGA Mobile PRC Laboratory Clinics Medical Truck (9)

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 (≥4.2M²), a reagent preparation area (≥2.6M²), a sample preparation area (≥5.8M²), an amplification area (≥3.5M²), and a cleaning and disinfection room (≥2.7M²). Each area shall be independent and not directly connected. Each independent experimental area shall be equipped with a special buffer room (≥0.7M²) 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: ≥2500M³/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: 1~10¹⁰ 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: 10-10¹⁰ 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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