• Vhp Sterilization Equipment Pharmaceutical Cleanroom H2O2 Interface Sterilization System Jiehao&Spincle
  • Vhp Sterilization Equipment Pharmaceutical Cleanroom H2O2 Interface Sterilization System Jiehao&Spincle

Vhp Sterilization Equipment Pharmaceutical Cleanroom H2O2 Interface Sterilization System Jiehao&Spincle

Certification: GMP, ISO
Voltage: 220V
Computerized: Computerized
Warranty: 1 Year
After-sales Service: Provided
Application: Pharmaceutical, Clean Room, Lab
Customization:
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  • Overview
  • Product Description
  • Product Parameters
  • Company Profile
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Overview

Basic Info.

Model NO.
ST-ISS-S100
Sterilization Concentration Curve Range
0-2000ppm
Power Supply
AC220V 50Hz
Sterilization Ability
6log
Sterilizing Solution
30~35% (H2O2)
Maximum Support Space
300m3
Control Method
PLC
Transport Package
Wooden Crate
Trademark
1000*500*800
Origin
China
Production Capacity
50sets/Year

Product Description

Product Description

With its mobile design and versatility, the VHP Cvcle SYSTEM is the most versatile hydrogen peroxide biocidal device on the market today. It utilizes our patented and innovative sterilization process. The process uses a hydrogen peroxide solution as a broad-spectrum antimicrobial agent with no condensation of the active ingredient. It has a wide range of material compatibility.
 

With unique design advantages
The whole machine is composed of stainless steel. Suitable for most environments Built-in steam generator can vaporize ≤35% hydrogen peroxide solution, which is delivered by high velocity airflow from high pressure fan. The software runs automatically to complete the selected biocidal cycle. The cycle is carried out in the following stages.
1,Dehumidification
Dry HEPA-filtered air is circulated to reduce humidity to a predetermined level within the 10-60% RH range. This allows the necessary H20:Christine vapor concentration to be kept below saturation (dew point) during the conditioning and sterilization phase. The return air passes through a dryer and is then heated and used as a carrier for the VHP. An internal HEPA filter prevents contamination of the internal Murata components and recontamination of the sealed chamber.

2,Conditioning Action
The HEPA-filtered dry air stream continues to flow as the H202 sterilizing steam is injected through the air stream before it leaves the unit.The H02 sterilant injection rate can be controlled in the range of 1 to 12 g/min. The conditioning phase helps to achieve the target biocidal concentration more quickly in larger volume sealed chamber applications. The conditioning time is affected by the sterilant injection rate, cavity volume, cavity contents and temperature.

3,Biological Sterilization
The target VHP sterilizing vapor concentration is maintained throughout the sealed chamber for a specific period of time, which varies depending on the structure of the sealed chamber and the chamber contents.

4,Catalytic degradation
The H20 sterilizing steam injection is stopped and the dry HEPA filtered air recirculation flow continues through the catalytic converter to reduce the H0 steam concentration in the chamber. A chamber exhaust system can also be used to accelerate degradation time.
 
Vhp Sterilization Equipment Pharmaceutical Cleanroom H2O2 Interface Sterilization System Jiehao&Spincle

Advantages of the VHP Cycle SYSTEM
Better performance
It has a more efficient vapor generator that quickly vaporizes the H20:solution, with significant proximity removal and drying capabilities. If you want to prove it, just compare our solutions to similar products and the VHP Cvcle SYSTEM wins, one comparison at a time.

Manipulability
Provides precise control of the biocidal unit as required by Good Manufacturing Practice (GMP) and allows operator, supervisor, attendant and administrator level access to the operation and process development of the biocidal unit.

Continuously stabilized high air pressure and volume
When air pressure is insufficient for effective drying and biocidal cycling, the VHFCycle SYSTEM provides both high air pressure and high air volume - both without compromise.

Audit Trail
Electronic Data Security 21 CFR Part 11 - Software features that support audit trails, electronic data capture/transmission, and other features used to verify and comply with 21 CFR Part 11.
 

Product Parameters
Model ST-ISS-S100
Externalsize(W*D*H) 1000mm*500mm*800mm
material SUS304L
Sterilization chamber temperature 27~35ºC
Sterilization chamber humidity 50~60%
Sterilization concentration 200-350PPM(Based on D-value)
Residual concentration values after sterilization ≤1PPM
Noise level ≤70db
Sterilization effffect 6log
Control host Siemens PLC
Communication method RS232 RS485 TCP/IP
Operation method HMI(Human Machine Interface/Physical Buttons)
Temperature and humidity monitoring -20ºC~250ºC,RH 0~100%
Concentration monitoring 0~2000ppm
Three levels of authority System Administrator, Operator Administrator, Operator
Hydrogen Peroxide 35% concentration of food-grade hydrogen peroxide solution
After-sales service Yes
Installation Services Additional quotations are required for difffferent regions and countries

 

Company Profile

Vhp Sterilization Equipment Pharmaceutical Cleanroom H2O2 Interface Sterilization System Jiehao&SpincleVhp Sterilization Equipment Pharmaceutical Cleanroom H2O2 Interface Sterilization System Jiehao&Spincle

Certificate

Vhp Sterilization Equipment Pharmaceutical Cleanroom H2O2 Interface Sterilization System Jiehao&Spincle

Packaging & Shipping

Vhp Sterilization Equipment Pharmaceutical Cleanroom H2O2 Interface Sterilization System Jiehao&Spincle

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Gold Member Since 2023

Suppliers with verified business licenses

Manufacturer/Factory & Trading Company
Registered Capital
739010.91 USD
Plant Area
1000 square meters