FDA UDI In Commercial Distribution 🇺🇸 United States

PureBliss

DI: D79010217051 · Model: 1021705 · PURELIFE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
PureBliss
Primary DI
D79010217051
Version / Model
1021705
Catalog Number
1021705
Company Name
PURELIFE, LLC
Labeler DUNS
828690904
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-09-22
Public Version
1
Public Version Date
2023-10-02
Public Version Status
New
Public Device Record Key
334cdb2b-2e8d-4752-ab1e-9775e536413a

Device Description

PureBliss Latex Powder-Free, X-Large, PureLife donates a portion of the proceeds from the sale of this glove to health and environmental causes, Fully-textured, Polymer-coated for an easy fit, Packaging contains at least 85% recycled material

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LYY Latex patient examination glove

GMDN Terms

Code Name
47172 Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Unit of Use D79010217050
Primary D79010217051

Customer Contacts