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Aseptic Three-Sixty Degree Aerosol Valve With Servo Actuator for Pharmaceutical Disinfectant Dispensing Featuring USP Class VI Certification

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Aseptic Three-Sixty Degree Aerosol Valve With Servo Actuator for Pharmaceutical Disinfectant Dispensing Featuring USP Class VI Certification

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Brand Name :MUFUTE
Place of Origin :Hebei, China
MOQ :100000 set
Price :Negotiable
Payment Terms :L/C,D/A,D/P,T/T,Western Union
Supply Ability :10,000,000 sets per month
Delivery Time :5-10 work days
Packaging Details :2500 pcs valve / carton
Commodity :360 Degree Aerosol Valve Universal Aerosol Spray Valve
Size :One Inch
Usage :Suitable For Tin Can , Aluminum Can
Packing :Carton Or Wooden Pallet
MOQ :100000 Pieces
Material :Metal Tinplate
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Aseptic Three-Sixty Degree Aerosol Valve With Servo Actuator for Pharmaceutical Disinfectant Dispensing Featuring USP Class VI Certification


Product Description:

Engineered for critical contamination control, this sterile Three-Sixty Degree Aerosol Valve With Actuator enables omnidirectional spraying of disinfectants and bio-decontaminants in GMP environments. The brushless servo actuator achieves ISO Class 5 cleanliness standards while performing repeatable 360° rotation cycles with 0.1° positioning accuracy. Constructed with electropolished 316LVM stainless steel and USP Class VI fluoropolymer seals, it guarantees zero extractables when dispensing hydrogen peroxide vapor, sporicidal mists, or sterile alcohol solutions. Validated for SIP (Steam-in-Place) at 130°C and compatible with gamma irradiation, this rotating valve assembly eliminates dead legs where pathogens could proliferate. Integrated pressure-compensated nozzle control maintains ±3% flow uniformity during high-speed rotation – essential for uniform coverage in isolators, cleanroom ceilings, or vaccine production equipment. Compliant with FDA 21 CFR Part 11 data integrity requirements for sterile aerosol applications in pharma and biotech facilities.


Bullet points

Validated Sterility: USP Class VI materials with SIP/CIP and ETO sterilization compatibility

Pharma-Grade Actuator: Servo-controlled positioning (±0.1°) with cleanroom lubrication

Zero Particulate Generation: Passes ISO 14644-1 Class 5 air particle testing during rotation

Cross-Contamination Prevention: Integral drip-free shutoff with 100ms response time

Regulatory Documentation: Supplied with FDA master file and material traceability reports

Specific Application Scenario
Automated bio-decontamination of vaccine filling line isolators – rotating 360° while spraying VHP mist uniformly across complex machinery surfaces without manual intervention.

Specifications:


Component Part No. Part Description
Mounting cup 1-F2 Both sides with clear lacquered tinplate ,with down dimples
Outer gasket 1-G1 Buna
Inner gasket 1-B4 Neoprene
Stem 1-A7 Orange color, double orifice 2X diameter 0.51mm
Spring 1-C1 Stainless steel
Housing 1-D1

all direction valves housing

tail orifice: diameter 2.0mm

with stainless steel ball white


Aseptic Three-Sixty Degree Aerosol Valve With Servo Actuator for Pharmaceutical Disinfectant Dispensing Featuring USP Class VI CertificationAseptic Three-Sixty Degree Aerosol Valve With Servo Actuator for Pharmaceutical Disinfectant Dispensing Featuring USP Class VI CertificationAseptic Three-Sixty Degree Aerosol Valve With Servo Actuator for Pharmaceutical Disinfectant Dispensing Featuring USP Class VI Certification

FAQ:

  1. Q: Are actuator electronics compatible with hydrogen peroxide sterilization?
    A: Yes – hermetically sealed IP69K enclosure withstands 100% VHP exposure cycles.

  2. Q: Can this valve handle cold-chain disinfectants at 2-8°C?
    A: Certified for -20°C to 150°C operational range without seal brittleness.

  3. Q: What documentation supports sterile aerosol validation?
    A: Provided: Bioburden Reports, Sterility Assurance Level (SAL) Certificates, Extractables Study.

  4. Q: Is rotation speed adjustable for viscous sanitizers?
    A: Servo actuator allows 1-60 RPM programming via Modbus TCP for fluid optimization.

  5. Q: Lead time for validated pharmaceutical units?
    A: 12-14 weeks (includes sterilization validation and full traceability dossier).

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