5 BOXES of 100 X-Small Halyard PureZero Black Nitrile Exam Gloves LFS711XS

HALYARD* PUREZERO* BLACK (9.5″) Nitrile Exam Gloves are designed for Medical, Dental, Veterinary, Ophthalmology, Tattoo, Piercing, Life Sciences, Forensics, Automotive, Janitorial, Food & Beverage, Industrial, Machinery & Equipment, EMS, Utilities, Warehousing, Healthcare, and Laboratories. HALYARD* PUREZERO* BLACK Nitrile Exam Gloves are tested for use against 15 chemotherapy drugs and 45 chemicals.

These gloves have also been tested and shown to have low dermatitis potential and no added/non-detectable levels of residual chemicals, including accelerators and contact sensitizers. The beaded cff allows for ease of donning, and fully textured glove surface provide tactile grip.

Features:

• Features a SMARTPULL* Dispenser to control dispensing and lessen waste
• Tested against 14 chemotherapy drugs fentanyl xylazine gastric acid and 44 chemicals.
• Powder-free and natural rubber latex-free
• Compliant for food handling applications
• AQL 1.5 (exceeds the ASTM standard of AQL 2.5 for critical defects or pinholes)
• 3 year shelf life
• Palm Thickness: 4.3 mil; Fingertip Thickness 5.1 mil
• Ambidextrous 9.5″. Beaded cuffs to prevent roll-down.

SMARTPULL* Dispenser

PUREZERO* BLACK gloves have a SMARTPULL* Dispenser, which incorporates two separate openings on the box. The first, smaller opening is used when the box is full to control dispensing and lessen waste. When the box is half empty, the second, larger opening allows easier access to the gloves.

Storage Instructions

HALYARD* PUREZERO* Nitrile Gloves shall be stored in conditions where the product is kept dry (away from moisture), away from direct sunlight, away from sources of heat, and away from radioactive sources.

Quality & Regulatory Standards

Compliant to quality management systems:

• ISO 9001: 2015
• ISO 13485: 2016
• US FDA 21 CFR part 820

Compliant to these biocompatibility standards:

• ISO 10993-10
• ISO 10993-11

Compliant to these food handling regulations:

• US FDA 21 CFR 177.2600 and US FDA CFR 180.22

Compliant to these medical device regulations:

• US FDA 21 CFR 880.6250 (510 (k) cleared device)

Compliant to these standards:

• ASTM D6319-19:2023
• ASTM F739-20:2020
• ASTM D6978-05: 2019
• ASTM F1671-07:2010
• Modified Draize – 95
• ASTM E1252-98: 2021