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PRODUCT

VHP  pass box sterilizer for pharmaceutical clean room car-t
VHP  pass box sterilizer for pharmaceutical clean room car-t VHP  pass box sterilizer for pharmaceutical clean room car-t VHP  pass box sterilizer for pharmaceutical clean room car-t

VHP pass box sterilizer for pharmaceutical clean room car-t

Product Attributes :

VHP technology refers to the low-temperature sterilization technology of vaporizing liquid hydrogen peroxide into hydrogen peroxide vapor and using vaporized hydrogen peroxide to sterilize the surface of objects.

Product Description

VHP  pass box sterilizer for pharmaceutical clean room car-t

VHP has a broad spectrum of bactericidal properties and can effectively kill all types of microorganisms such as bacteria, fungi, molds, viruses, bacterial spores, etc. It is currently found that the most difficult microorganisms to kill with VHP are thermophilic fat spores, so the biological indicator used for VHP sterilization validation is thermophilic fat spores.

 

• VHP sterilization is non-toxic and has no residue. Vaporized hydrogen peroxide can quickly kill microorganisms during the sterilization process. After sterilization, it can quickly degrade into H20 and 02, which is non-toxic and has no residue, and the residual concentration of hydrogen peroxide can be detected.

 

VHP  pass box sterilizer Product Principle

• The sterilization effect of VHP can be verified. A normal validation cycle includes parameter development, VHP distribution research, biological challenge test and exhaust degradation research. The vaporized hydrogen peroxide equipment has a complete GMP validation document system.

• VHP sterilization has good compatibility. The vaporized hydrogen peroxide sterilizers adopt a unique saturation control method to ensure that hydrogen peroxide does not liquefy or condense during the entire sterilization process, and the material compatibility is better.

Equipment body

The VHP transfer cabin adopts a stainless steel main structure, the inner cavity adopts 316L stainless steel, the frame and outer surface adopt 304 stainless steel structure, the inner cavity adopts a rounded corner full welding design, and adopts a Ra≤0.6um polishing degree.

VHP generation unit

The dry VHP generator based on the flash evaporation principle adopts an integrated control method and adopts a unified control method with the VHP transfer window. The VHP generation concentration, cavity temperature, humidity, and saturation control are more stable.

Pneumatic sealing system.

 

The compressed air power system includes the control of the inflatable seal and the pneumatic valve. The inflatable seal and pneumatic valve control use a compressed air pipeline, including a pressure-reducing valve and a solenoid valve control. The other compressed air is controlled by an independent pressure-reducing valve and a solenoid valve for cavity saturation control.

 

 

Model

Inner size (W*D*H)

External size (W*D*H)

Powe (kw)

 

HPB-216

600*600*600mm

1050*650*1800mm

2.0

 

HPB-288

600*600*800mm

1050*650*2000mm

2.2

 

HPB-360

600*1000*600mm

1050*1050*1800mm

2.2

 

HPB-512

800*800*800mm

1250*850*2000mm

2.3

 

HPB-640

800*800*1000mm

1250*850*2200mm

2.5

 

HPB-800

800*1000*1000mm

1250*1050*2200mm

2.6

 

HPB-960

800*1000*1200mm

1450*1250*2150mm

2.8

 

HPB-1536

800*1200*1600mm

1450*1250*2150mm

3.0

 

HPB-1792

800*1400*1600mm

1450*1450*2150mm

3.2

 

HPB-2688

1200*1400*1600mm

1850*1450*2150mm

4.0

 

Note: The above are standard products, non-standard products can consult our sales staff, we can provide non-standard customized products according to customer requirements.

VHP pass box sterilizer Common material introduction

 

Item

Power

Compressed air

Exhaust

Requirements

220v/50/Hz

6-8Bar, RH%<30% clean compressed air

Interface DN50 stainless steel pipe, Ø64mm flange quick clamp

•ASME BPE process pipeline: The process pipeline is made of 316L stainless steel, and provides ASME BPE-compliant joint logs and reports.
•Audit trail: Siemens Audit trail module and authorization are used to achieve FDA-compliant audit trail requirements.
•Electronic signature: The function complies with 21CFR Part11, which is generally required for FDA standard projects.
•Bio seal: Complies with BSL-3 or BSL-4 bio seal requirements and is selected for biosafety projects.
•GMP verification (FAT, SAT, DQ, IO/PQ): Verification documents and services that meet GMP requirements can be purchased according to needs.
•ZSZ: Parts and consumables used for daily or regular maintenance of equipment, including inflatable seals, silicone tubes, VHP concentration probes, etc.
•Loading car: 304 stainless steel material, used for the transportation of cavity loading brackets, easy to use.
•VHP low concentration probe: installed on the exhaust duct to detect the VHP concentration at the end of sterilization.
•Clean side operation screen: realizes double-sided operation and observation of the equipment for easy use.
•TCP/IP network port: used for electronic data transmission and connection of equipment to SCADA system.
•Venturi nozzle: assists the distribution of hydrogen peroxide inside the large cavity VHP transfer window to achieve a better distribution effect.