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Sterile SatPax® MicroSeal® WFI Presaturated Nonwoven Cleanroom Wiper, Berkshire
Sterile SatPax® MicroSeal® WFI Presaturated Nonwoven Cleanroom Wiper, Berkshire
Catalog # 89089-432
Supplier:  Berkshire
Small Business Enterprise
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Sterile SatPax® MicroSeal® WFI Presaturated Nonwoven Cleanroom Wiper, Berkshire
Catalog # 89089-432
Supplier:  Berkshire
Supplier Number:  SSPMS01.5WFI
Small Business Enterprise

Specifications

  • Fibres (>100 µm):
    150/cm²
  • Extractables:
    0.038% using deionized water, 0.0083% using isopropyl alcohol
  • Basis weight:
    72.1 g/m²
  • Particle generation (>=0,5 µm):
    26 x 10³/m²
  • Absorbency - extrinsic:
    329 ml/m²
  • Absorbency rate:
    3 sec.
  • Absorbency - intrinsic:
    4.6 ml/g
  • Ions - calcium:
    2 ppm
  • Ions - magnesium:
    1.3 ppm
  • Ions - potassium:
    0.46 ppm
  • Ions - sodium:
    16 ppm
  • Cat. no.:
    89089-432
  • W×L:
    30.5×30.5 cm (12×12)"
  • Supplier No.:
    SSPMS01.5WFI

Specifications

About this item

Sterile SatPax® MicroSeal® WFI combines MicroSeal® 1200 ultrasonically sealed-edge cleanroom laundered wipers composed of 100% continuous filament polyester knit fabric with a high saturation level of 70% IPA and 30% WFI. This pre-wetted format provides a cost effective and easy to use solution versus traditional bulk handling of solvents.

  • 100% continuous filament polyester knit
  • Ultrasonically sealed edge for reduced fiber contamination
  • Laundered and packaged in Berkshire’s ISO Class 4 cleanroom
  • Triple packaged for easy entry into sterile environments
  • Re-sealable solvent resistant packaging

Solvent is 70% isopropyl alcohol and 30% water for injection (WFI). No chemical binders in base material. Suitable for ISO Class 3 (FED-STD-209E Class 1/M1.5) and less critical environments. Excellent for wet cleaning of critical surfaces where control of flammable solvents and flammable solvent concentrations is required.

Certifications: Gamma irradiated to a Sterility Assurance Level of 10⁻⁶ per AAMI guidelines. Certificate of sterility. Passes LAL test for endotoxins <20 EU/device. Complies with RoHS and REACH requirements. Meets cGMP requirements for traceability. Laundered and packaged in an ISO Class 4 (FED-STD-209E Class 10/M2.5) cleanroom.
Ordering information: Packaged in resealable, solvent-resistant packaging.