FDA UDI In Commercial Distribution 🇺🇸 United States

PureOnyx

DI: D79010681031 · Model: 1068103 · PURELIFE, LLC
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
PureOnyx
Primary DI
D79010681031
Version / Model
1068103
Catalog Number
1068103
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
150bcd8b-d6e3-44a1-a91e-36334e181b8a

Device Description

PureOnyx Black Nitrile Powder-Free, Medium, Nitrile powder-free gloves, Textured fingertips, Black in color, Packaging contains 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
No
Not Made with NRL
Yes
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
QDO Fentanyl and other opioid protection glove
LZC Medical Glove, Specialty
LZA Polymer patient examination glove

GMDN Terms

Code Name
56286 Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Unit of Use D79010681030
Primary D79010681031

Customer Contacts