T-Style Isolation Gown, LLDPE, Large, Light Blue, 50/Carton

  • Easy to put on and take off.
  • Gap in end of sleeve seal for fingers/hand.
  • Back side is marked and perforated for easy removal.
  • Made from polyethylene (Virgin LLDPE).
  • Long sleeve, full coverage, one-size.
  • Not sterilized, for non-surgical use only.
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SKU: HERTGOWNLP Category: Tag:

Polyethylene, non-surgical isolation gowns are easy to put on and take off. Back side is marked and perforated for easy removal. Gap in end of sleeve seal for fingers/hand. Full length, long sleeve style provides full coverage. Polyethylene, non-surgical isolation gowns are easy to put on and take off. Back side is marked and perforated for easy removal. Gap in end of sleeve seal for fingers/hand. Full length, long sleeve style provides full coverage. This Class I device has not been FDA cleared or approved. Not intended for antimicrobial or antivirus protection, infection prevention, or infection reduction, surgical use and is not sterilized. Single use only. Do not use in the presence of any high intensity heat source or flammable gas. Authorized by the FDA under an Emergency Use Authorization for use as PPE in health care settings as they may help protect HCPs and/or patients from the transfer of viruses in low or minimal risk level situations. Apparel Type: Isolation Gown; Material(s): LLDPE; Color(s): Light Blue; Color Family: Blue.

HERTGOWNLP
HER-TGOWNLP

Additional information

Brand

HERITAGE

Apparel Type

Isolation Gown

Global Product Type

Isolation Gowns

Material(s)

LLDPE

Color(s)

Light Blue

Color Family

Blue

Size Group

Large

Washable

No

Suggested Use

Non-Surgical Healthcare

Product Biodegradability Indicator

N

Product Compostability Indicator

N

Compliance Standards

Tested for Compliance with ANSI/AAMI PB70:2012 Minimal Barrier Performance Level 1, Level 2 Requirements

Pre-Consumer Recycled Content Percent

0%

Post-Consumer Recycled Content Percent

0%

Total Recycled Content Percent

0%

Disclaimer Statement

This is a Class I device and has not been FDA cleared or approved.

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