Surgicare Plus Sterile Latex Surgical Gloves Powder Free for Industrial Use - 50 Pairs (1 Box)

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Surgicare Plus Sterile Latex Surgical Gloves Powder Free for Industrial Use - 50 Pairs (1 Box)

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Specifications

  • Product Name : Powder Free Sterile Latex Surgical Gloves
  • Material : Natural Rubber Latex
  • Colour : White to Pale Yellow
  • Shape : Anatomic
  • Cuff : Beaded
  • External Surface : Textured
  • Internal Surface : Chlorinated
  • Size : 5.5, 6.0, 6.5, 7.0, 7.5, 8.0, 8.5 and 9.0
  • Sterilization : Ethylene Oxide (EO) / GAMMA (R)
  • Shelf Life : 3 years
  • Basic UDI-DI : 806363LSGFM4

highlights

  • Eliminates powder-related complications
  • Reduces risk of surgical site contamination
  • Comfortable for prolonged wear
  • Provides strong barrier protection
  • Available in multiple sizes for optimal fit

in the box

  • Surgicare Plus Sterile Latex Surgical Gloves Powder Free

Quality :

  • 100% Inspected.
  • AQL 0.65 for pin holes

Standards :

  • ASTM D 3577-19 (2023)
  • EN 455-1:2020+A2:2024
  • EN 455-2:2024
  • EN 455-3: 2023
  • ISO 10282:2023
  • IS 13422:2024
  • ASTM F 1671:2022
  • Registered with US FDA (510K)
  • CE Mark-Medical device Class IIa/PPE Cat. Ill

Use Cases :

  • General and specialized surgical procedures
  • Operation theatres (OT)
  • Minor and major surgeries
  • Dental surgical procedures
  • Clinical and hospital environments

Safety Features :

  • Latex protein no more than 50μg of protein per gram and dm², eliminates risk of Latex Allergy - Type 1.
  • Chemical residue almost nil, eliminates risk of Contact Dermatitis - Type IV Allergy.
  • Absence of powder eliminates dangers associated with powder, preventing granulomas, adhesions, fibrosis and occupational asthma. Does not contaminate sterile work area.
  • Latex film structure passes Viral Penetration Test (ASTM F1671:2013)
  • Manufactured in clean environment to reduce bio-burden level prior to sterilization. This achieves low Pyrogen level after sterilization.
  • Manufactured in a clean environment to comply with EN 556 & ISO 13485 requirements.
  • Sterilized in a validated process cycle to achieve sterility assurance level of 10⁻⁶, and air wash cycles to reduce sterilant residue to less than 4mg/unit.

Warranty

No Warranty

Seller

AA MEDIE QUIPLearn More

Product Description

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