Single use valves for powder transfer

Efficiently transfer powder ingredients with a single-use containment solution, ensuring sterility while reducing the need for costly cleaning and validation processes. Ideal for maintaining product integrity in complex manufacturing environments.

Transfers and Contains Pharmaceutical Powders

The Single Use Split Butterfly Valve Passive by ChargePoint Technology is an innovative solution specifically designed for the seamless transfer of pharmaceutical powders, ensuring stringent containment and sterility. This disposable valve integrates into your production line as the passive mating half of the ChargePoint Split Butterfly Valve system. It excels in aseptic processing, eliminating cleaning and maintenance burdens while maintaining high containment levels. Constructed from FDA and USP Class VI compliant plastics, it accommodates both sterile and non-sterile applications. Perfect for pharmaceutical, biotech, and chemical industries, this valve supports various applications, including powder transfer, chemical synthesis, and solid dose formulation. Supplied sterilized and ready for use, the valve ensures efficiency, supporting compliance with GMP standards. Its design allows for a swift, secure connection during powder handling, making it a practical choice for facilities prioritizing speed, safety, and sterility.

Benefits

  • Enhances operational efficiency by eliminating cleaning and maintenance needs.
  • Ensures sterility and contamination prevention in aseptic processing.
  • Facilitates cost-effective single-use applications with disposable design.
  • Complies with GMP standards, ensuring regulatory compliance.
  • Simplifies integration into existing systems with versatile connection options.

General


Applications
Bioprocessing,Fine chemicals,Pharmaceutical powder,Biopharmaceuticals,Aseptic processing,Chemical synthesis,Solid dose formulation
End products
Chemical actives,Vial stoppers,Active pharmaceutical ingredients (apis),Chemical intermediates,Buffer media,Tablets,Excipients,Capsules
Steps before
Powder synthesis,Solid dose formulation,Bioprocessing media preparation
Steps after
Aseptic processing,Sterilization,Packing
Input ingredients
powder ingredients,pharmaceutical powders,buffer/media powder,API,excipients,formulations
Output ingredients
processed powder ingredients,formulated tablets,formulated capsules,aseptically processed powders
Market info
Chargepoint Technology is known for its expertise in designing and manufacturing high containment and sterile transfer solutions for pharmaceutical and biopharmaceutical industries, particularly in powder containment and aseptic transfer systems.

Technical Specifications


Compliance
FDA and USP Class VI
Sterilization method
Gamma sterilised
Material
Plastic
Connection type
Tri-clamp connection ferrule
Cleanroom Standards
ISO6
Weight
Lightweight
Usage
Single use
Versions
Sterile and Non-sterile
Packaging
ChargeBag® PE-S integration
Function
Passive mating half
Security accessory
Lockable GMP cover

Operating Characteristics


Working Mechanism
Split Butterfly Valve System
Docking Procedure
Passive and Active Unit Docking
Batch vs. Continuous Operation
Batch Operation
Cleaning Requirements
Not Required (Single Use)
Sterilization Method
Gamma Sterilized
Containment Level
High Containment Performance
Material Composition
FDA and USP Class VI Compliant Plastic
Lockable Security
GMP Cover Available

Material Compatibility


Biological compatibility
FDA and USP Class VI compliant
Cleanability
Disposable,no cleaning required
Compatibility with pharmaceuticals
High
Chemical resistance
Gamma sterilised,suitable for aseptic processing
Corrosive resistance
Resistant to degradation in cleanroom conditions
Density/particle size
Powder transfer applications

Product type Characteristics


Container integration
ChargeBag® PE-S
Containment performance
High
Powder transfer
Pharmaceutical / Biotech

Physical Characteristics


Material
FDA and USP Class VI compliant plastic
Weight
Lightweight
Design
Disposable version of the passive mating half
Connection option
Tri-clamp connection ferrule
Construction
Supplied gamma sterilised
Cleanroom classification
ISO6 cleanroom environment

Custom Options


Disposable version
Single use
Sterilization method
Gamma sterilized
Material
FDA and USP Class VI compliant plastic
Connection type
Tri-clamp / welded
Version type
Sterile / Non-sterile