FDA UDI In Commercial Distribution 🇺🇸 United States

PureBerry

DI: D79010671031 · Model: 1067103 · PURELIFE, LLC
Product Codes
3
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
PureBerry
Primary DI
D79010671031
Version / Model
1067103
Catalog Number
1067103
Company Name
PURELIFE, LLC
Labeler DUNS
828690904
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2021-03-22
Public Version
1
Public Version Date
2021-03-30
Public Version Status
New
Public Device Record Key
12604567-2ac6-4257-9390-a8fff6a24be5

Device Description

Medium, Nitrile powder-free gloves, Textured fingertips, Berry-blue 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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LZA Polymer Patient Examination Glove
LZC Patient Examination Glove, Specialty
QDO Fentanyl And Other Opioid Protection Glove

GMDN Terms

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

Identifiers

Type ID
Package D79010671033
Primary D79010671031
Unit of Use D79010671030

Customer Contacts

Phone
877-777-3303