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SterileWipe® LP-10 Sterile Dry Wipers Ultra-Low Particle Sterile Polyester Wipers for Critical Aseptic Processing SterileWipe® LP-10 wipers are engineered from continuous filament polyester with ultra-low particle generation and validated sterility, delivering consistent, high-purity performance for the most demanding aseptic and cleanroom environments. ▼ EXPAND TECHNICAL REFERENCE
Next-Level Low Particle Control for Sterile Environments
SterileWipe® LP-10 wipers are constructed using high-quality continuous filament polyester designed to minimize particle shedding and fiber release. The LP-10 platform represents an elevated low-particle standard for environments requiring tighter contamination thresholds.
Each wipe is cleanroom laundered and terminally sterilized via validated gamma irradiation, ensuring a defined sterility assurance level (SAL). Multi-layer cleanroom packaging supports aseptic transfer and maintains sterility integrity during use.
SterileWipe® LP-10 is ideal for pharmaceutical manufacturing, biotechnology processes, and advanced cleanroom environments where both sterility and ultra-low particulate levels are required.
Sterility & Ultra-Low Particle Construction
Gamma Sterilized:
Validated sterilization ensuring consistent sterility assurance levels (SAL).
Continuous Filament Polyester:
Minimizes particle generation and fiber release.
Enhanced LP-10 Structure:
Further reduces particulate contamination compared to standard LP wipes.
Cleanroom Laundered:
Removes contaminants prior to sterilization.
Multi-Layer Packaging:
Supports aseptic transfer and maintains sterility integrity.
Fast Selection Guidance
  • Ultra-critical aseptic environments: ideal for tight contamination limits.
  • ISO Class 3–5 cleanrooms: ultra-low particle performance.
  • Pharmaceutical manufacturing: supports GMP and validated processes.
  • Biotechnology applications: high-purity contamination control.
  • Precision cleaning: safe for sensitive and critical surfaces.
  • Advanced processes: choose LP-10 for elevated cleanliness standards.
SterileWipe® LP-10 Performance Considerations
  • Particle Control: extremely low lint and particulate generation.
  • Sterility Assurance: validated SAL for aseptic applications.
  • Extractables: low NVR and ionic contamination levels.
  • Durability: maintains integrity during wet and dry use.
  • Absorbency: controlled fluid handling for precision cleaning.
  • Surface Compatibility: safe for sensitive and high-value components.
  • Process Consistency: supports validated and repeatable workflows.
Typical Applications
  • Aseptic filling and sterile processing environments
  • Pharmaceutical and biotechnology cleanrooms
  • ISO Class 3–5 cleanroom operations
  • Advanced microelectronics and precision manufacturing
  • Critical equipment and surface cleaning
  • High-purity contamination control programs
  • Surface preparation and disinfection
  • Validated cleanroom cleaning protocols
Common Ultra-Low Particle Sterile Wiper Issues to Avoid
  • Using standard sterile wipes where ultra-low particle control is required.
  • Improper aseptic transfer compromising sterility.
  • Assuming all low-particle wipes perform equally.
  • Opening packaging outside controlled environments.
  • Using lower-grade wipes in critical applications.
  • Not aligning wipe selection with process validation requirements.
SterileWipe® LP-10 Category Path
This category sits within Sterile Dry Wipers and represents SterileWipe® LP-10 products engineered for ultra-low particle generation and validated sterility. It is best suited for the most critical aseptic environments requiring maximum contamination control and process reliability.
Need Help Selecting the Highest Purity Sterile 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, particle control standards, and process validation. Customers are responsible for verifying suitability within their specific aseptic environment.