FDA UDI In Commercial Distribution 🇺🇸 United States

PremierPro

DI: 00818566010353 · Model: 5072 · PRESTIGE AMERITECH, LTD.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
PremierPro
Primary DI
00818566010353
Version / Model
5072
Catalog Number
5072
Company Name
PRESTIGE AMERITECH, LTD.
Labeler DUNS
199692794
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-26
Public Version
2
Public Version Date
2026-03-23
Public Version Status
Update
Public Device Record Key
94b78d66-122f-4a6a-b9aa-d71629a38956

Device Description

PremierPro Sterile Nitrile Exam Glove Single Small

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LZC Patient Examination Glove, Specialty
LZA Polymer Patient Examination Glove

GMDN Terms

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

Identifiers

Type ID
Package 00818566010544
Primary 00818566010353
Package 10818566010350

Customer Contacts