PowerChem® PC-045-095GR Green Neoprene Exam Gloves, 3.5 mil, case/1000

$124.53

Description

High performance neoprene gloves provide superior resistance to chemicals, punctures, and abrasion.
Features:

Silicone-free for critical environments
Exceeds 1.5 AQL laboratory standards
SHA Dermatologically Approved
Optimal thickness for durability and tactile sensitivity
Latex-free pure neoprene
Tear-resistant beaded cuff for easy donning

Properties:

Inner Surface: Smooth
Outer Surface: Textured
Cuff: Finish Beaded
Fit Type: Ambidextrous
Length: 9.5″ / 242 mm
Finger Thickness: 3.5mil / 0.09mm
Palm Thickness: 2.8mil / 0.07mm
Tensile Strength Before Aging: 14 MPa
Tensile Strength After Aging: 14 MPa
Elongation Before Aging: 500%
Elongation After Aging: 400%
AQL: 1.5

Compliance:

EN ISO 21420:2020
EN 455:2000-2015
ASTM D6977-19
Reach EU 1907/2006
EU 2016/425
FDA 21 CFR 177.2600

 
Viral Protection
SW gloves have been successfully tested against the stringent US and EU viral penetration test standards, thus giving stakeholders a high level of protection from viruses, bacteria and fungi. This reduces or eliminates the risk of exposure to biological hazards and guarantees quality of every glove produced. ASTM F1671 is the standard used in North America. It is a pass or fail test designed to show whether the material can protect a wearer from viruses transmitted via blood or bodily fluids. EN ISO 374-5 Virus standard, is the standard in Europe. It measures the ability of gloves to protect from bacteria, fungi and virus penetration using ISO 16604 as the test method.
SKIN HEALTH ALLIANCE APPROVED WORLDWIDE
SW® nitrile gloves have been clinically tested and proven to have reduced potential to cause skin irritation. This protection creates a cleaner glove with reduced chemical residues, removes the user’s risk of allergic reactions, and will not induce contact dermatitis or Type IV hypersensitivity reaction.& To achieve a 510K Certification, a medical grade glove must meet ASTM and FDA standards. Tested by an FDA registered and certified US laboratory and headed by a board-certified dermatologist. Testing was conducted on a minimum of 200 human subjects, to qualify for the Low Dermatitis Claim.

dermatologist tested
skin safe products
global standard adherence
low environmental impact
independently assessed

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