FDA UDI In Commercial Distribution 🇺🇸 United States

PremierPro

DI: 00818566010155 · Model: 2350 · PRESTIGE AMERITECH, LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
PremierPro
Primary DI
00818566010155
Version / Model
2350
Catalog Number
2350
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
fe79c239-8acf-41fd-8374-c8e4455679c5

Device Description

PremierPro PE Coated Cover Gown White, Neck Tie, Knit Cuff, Universal, 10count

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
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
OEA Non-Surgical Isolation Gown

GMDN Terms

Code Name
35492 Isolation gown, single-use

Identifiers

Type ID
Package 10818566010152
Primary 00818566010155

Customer Contacts