FDA UDI In Commercial Distribution 🇺🇸 United States

PremierPro

DI: 00818566010759 · Model: 83212B · PRESTIGE AMERITECH, LTD.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
PremierPro
Primary DI
00818566010759
Version / Model
83212B
Catalog Number
83212B
Company Name
PRESTIGE AMERITECH, LTD.
Labeler DUNS
199692794
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-25
Public Version
4
Public Version Date
2026-03-23
Public Version Status
Update
Public Device Record Key
028067e2-367d-4fa3-9e8c-2b2ba09b30e3

Device Description

PremierPro OR Towel, 17" x 24" Sterile, Blue, 12pk

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
Yes
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
KKX Drape, Surgical
PUI Drape, Surgical, Exempt

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Package 10818566010756
Primary 00818566010759

Customer Contacts