PureBliss 1021702

GUDID D79010217020

Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

Primary Device ID	D79010217020
NIH Device Record Key	5cfdc60b-cd2a-47d2-b324-f5574720f8b2
Commercial Distribution Status	In Commercial Distribution
Brand Name	PureBliss
Version Model Number	1021702
Catalog Number	1021702
Company DUNS	828690904
Company Name	PURELIFE, LLC
Device Count	100
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	true
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
HIBCC	D79010217020 [Unit of Use]
HIBCC	D79010217021 [Primary]

LYY	Latex patient examination glove

Steralize Prior To Use	false
Device Is Sterile	false

D79010217050	PureBliss Latex Powder-Free, X-Large, PureLife donates a portion of the proceeds from the sale o
D79010217040	PureBliss Latex Powder-Free, Large, PureLife donates a portion of the proceeds from the sale of
D79010217030	PureBliss Latex Powder-Free, Medium, PureLife donates a portion of the proceeds from the sale of
D79010217020	PureBliss Latex Powder-Free, Small, PureLife donates a portion of the proceeds from the sale of
D79010217010	PureBliss Latex Powder-Free, X-Small, PureLife donates a portion of the proceeds from the sale o