FDA UDI In Commercial Distribution 🇺🇸 United States

Nu Flex

DI: 00850058725666 · Model: 4504002 · Direct Marketing USA LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Nu Flex
Primary DI
00850058725666
Version / Model
4504002
Company Name
Direct Marketing USA LLC
Labeler DUNS
079327950
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-07
Public Version
1
Public Version Date
2024-05-15
Public Version Status
New
Public Device Record Key
dd8a53a9-8ffe-4067-a3cd-d6d23738a21d

Device Description

Blue Nitrile powder free exam glove 3.5 mil size med

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
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LZA Polymer Patient Examination Glove

GMDN Terms

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

Identifiers

Type ID
Primary 00850058725666
Package 10850058725618