FDA UDI In Commercial Distribution 🇺🇸 United States

Inteplast

DI: 00762935082024 · Model: NF205 · Inteplast Group Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Inteplast
Primary DI
00762935082024
Version / Model
NF205
Company Name
Inteplast Group Corporation
Labeler DUNS
786941427
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-11
Public Version
1
Public Version Date
2023-01-19
Public Version Status
New
Public Device Record Key
fcc8d1a0-c220-4e92-9338-bda0506740bc

Device Description

Nitrile exam grade powder free glove size XXL

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

GMDN Terms

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

Identifiers

Type ID
Primary 00762935082024
Package 07629350820248
Package 07629350820217