FDA UDI In Commercial Distribution 🇺🇸 United States

PremierPro

DI: 00818566010117 · Model: 2320 · PRESTIGE AMERITECH, LTD.
Product Codes
2
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
PremierPro
Primary DI
00818566010117
Version / Model
2320
Catalog Number
2320
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
2
Public Version Date
2026-03-23
Public Version Status
Update
Public Device Record Key
2aacc08b-ae11-469a-b8bd-2f7b4c8c220c

Device Description

PremierPro Blue Thumbloop Gown Universal 15count

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OEA Non-Surgical Isolation Gown
FME Gown, Examination

GMDN Terms

Code Name
32170 Professional examination gown, single-use
35492 Isolation gown, single-use

Identifiers

Type ID
Package 10818566010114
Primary 00818566010117

Customer Contacts