SterileWipe® AS-10 Sterile Dry Wipers Gamma-Sterilized Polyester Wipers for Aseptic and Critical Cleanroom Environments SterileWipe® AS-10 wipers are constructed from continuous filament polyester and terminally sterilized to provide ultra-low particle generation, low extractables, and validated sterility for aseptic processing environments. ▼ EXPAND TECHNICAL REFERENCE
Sterile Polyester Wipers for Aseptic Processing
SterileWipe® AS-10 wipers are engineered from continuous filament polyester to minimize particle shedding and fiber release, then terminally sterilized using validated gamma irradiation processes. This ensures consistent sterility assurance for use in critical environments.
These wipes are double or triple bagged in cleanroom-compatible packaging systems, allowing for staged transfer into controlled environments while maintaining sterility. Their low extractables profile supports sensitive pharmaceutical and biotechnology processes.
SterileWipe® AS-10 is commonly used in ISO Class 3–5 cleanrooms, aseptic filling suites, and sterile compounding environments where contamination control and sterility are essential.
Sterility & Material Construction
Gamma Sterilized:
Validated sterilization process with defined sterility assurance levels (SAL).
Validated sterilization process with defined sterility assurance levels (SAL).
Continuous Filament Polyester:
Ultra-low lint and particle generation for critical environments.
Ultra-low lint and particle generation for critical environments.
Low Extractables Profile:
Minimizes ionic and non-volatile residues.
Minimizes ionic and non-volatile residues.
Cleanroom Laundered:
Processed to remove contaminants prior to sterilization.
Processed to remove contaminants prior to sterilization.
Multi-Layer Packaging:
Supports aseptic transfer into controlled environments.
Supports aseptic transfer into controlled environments.
Fast Selection Guidance
- Aseptic environments: required for sterile processing areas.
- ISO Class 3–5 cleanrooms: ultra-low particle performance.
- Pharmaceutical manufacturing: supports GMP compliance.
- Sterile compounding: validated sterility assurance.
- Critical cleaning tasks: low extractables and high purity.
- Controlled transfer: multi-bag packaging for sterile entry.
SterileWipe® AS-10 Performance Considerations
- Sterility Assurance: validated SAL for aseptic applications.
- Particle Control: ultra-low lint and fiber release.
- Extractables: low NVR and ionic contamination levels.
- Durability: strong knit supports wet and dry use.
- Absorbency: efficient fluid handling for cleaning processes.
- Surface Compatibility: safe for sensitive equipment.
- Regulatory Alignment: supports GMP and controlled processes.
Typical Applications
- Aseptic filling and processing areas
- Pharmaceutical cleanrooms
- Biotechnology manufacturing environments
- Sterile compounding facilities
- ISO Class 3–5 cleanroom operations
- Critical equipment cleaning
- Surface disinfection and preparation
- Validated contamination control programs
Common Sterile Wiper Issues to Avoid
- Using non-sterile wipes in aseptic environments.
- Improper transfer techniques compromising sterility.
- Assuming all sterile wipes have equal SAL validation.
- Opening packaging outside controlled environments.
- Using wipes beyond validated sterility conditions.
- Not aligning wipe selection with regulatory requirements.
SterileWipe® AS-10 Category Path
This category sits within Sterile Dry Wipers and represents SterileWipe® AS-10 products engineered for aseptic processing and high-purity environments. It is best suited for applications requiring validated sterility, low extractables, and consistent contamination control performance.
Need Help Selecting the Right Sterile Cleanroom Wiper?
Contact our contamination-control specialists at Sales@SOSsupply.com or call (214) 340-8574.
SOSCleanroom Disclaimer
This information is provided for general educational purposes regarding sterile cleanroom wipers. Product selection should be based on sterility requirements, regulatory standards, and process validation. Customers are responsible for verifying suitability within their specific aseptic environment.