FDA UDI In Commercial Distribution 🇺🇸 United States

PrestigePro

DI: 00840490851054 · Model: 5105 · PRESTIGE AMERITECH, LTD.
Product Codes
3
GMDN Terms
1
Identifiers
2
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
PrestigePro
Primary DI
00840490851054
Version / Model
5105
Catalog Number
5105
Company Name
PRESTIGE AMERITECH, LTD.
Labeler DUNS
199692794
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-23
Public Version
1
Public Version Date
2025-07-01
Public Version Status
New
Public Device Record Key
f9060b67-18f7-4148-9723-964dc6e063d7

Device Description

PrestigePro Nitrile Extended Cuff Glove 12" XL, 50count

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 Medical Glove, Specialty
OPJ Medical Gloves With Chemotherapy Labeling Claims - Test For Use With Chemotherapy Drugs

GMDN Terms

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

Identifiers

Type ID
Package 50840490851059
Primary 00840490851054

Customer Contacts