PROFEEL®

DHD Double Gloving System Non-Latex, Sterile

P33xx-62
Exceptional Protection

Two pairs of gloves per pack: overgloves and undergloves.
Wearing two pairs of surgical gloves provide an additional barrier and further reduce the risk of contamination. Reduce the number of perforation to innermost pair of surgical gloves. Polyisoprene's intrinsic softness provides an exceptionally comfortable and flexible glove.
Damp Hand Donning (DHD™) - Inner surface of the glove is coated with a proprietary polymer to enhance damp hand donning.

A non slick skin-grip surface finish provides excellent instrument grip, under both wet and dry conditions. A superior tactile sensitivity provides optimum ‘feel’.
Specially designed high tack band near the cuff of the glove to securely hold onto the wearer’s gown to minimize roll down. A reinforced beaded cuff feature ensures easy donning while preventing tearing. Tested for water leak before packing to AQL 0.65.
The cuff is printed with size and logo for easy identification.

symbol-02.png

DHD Double Gloving System Non-Latex, Sterile Special

Type Overglow: Powder free, polymer coated, damp-hand-donnable (DHD™) and Gamma sterilzed.
Underglow: Micro thin, powder free, polymer coated, damp-handdonnable (DHD™) and Gamma sterilzed.
Primary Materials Polyisoprene
Powder ≤ 2
Color Overglow: Off White
Underglow: Green
Design and Feature Overglow: Hand Specific, curved fingers, bisque finish (SH3) and beaded cuff.
Underglow: Hand Specifc, curved fingers, smooth finish for easy double gloving and beaded cuff.
Surface Treatment Polymer coated on inner surface to ease donning. Outer surface is smooth.
Packing 1 pair of Overgloves and Undergloves per inner wrapper, 25 pouches per dispenser, 4 dispensers per carton.
Product Conformance
  • Personal Protective Equipment of Complex Design Category III, in compliance with European Regulation (EU) 2016/425, type tested to EN 420:2003+A1:2009, EN ISO 374-1:2016 Type B, EN 374-2:2014, EN 16523-1:2015, EN 374-4:2013 & EN ISO 374-5:2016,
  • CE Class IIa Sterile Medical Device, in compliance with 93/42/EEC, type tested to EN 455-1:2000, EN 455-2:2015, EN 455-3:2015, EN 455-4:2009
  • CE2797
  • ASTM D3577
Quality Assurance
  • US FDA Quality System Regulation (QSR)
  • ISO9001 Quality Mangement System
  • BS EN ISO13485 Quality Systems

  • Store in cool dry place
    Store in cool dry place
  • Do not expose to water
    Do not expose to water
  • Latex free
    Latex free
  • Single use only
    Single use only