FDA UDI In Commercial Distribution 🇺🇸 United States

PremierPro

DI: 00818566017512 · Model: 2396 · 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
00818566017512
Version / Model
2396
Catalog Number
2396
Company Name
PRESTIGE AMERITECH, LTD.
Labeler DUNS
199692794
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-24
Public Version
2
Public Version Date
2026-03-23
Public Version Status
Update
Public Device Record Key
fe65fe58-e21d-4af7-9840-fc30c1fc880b

Device Description

PremierPro PE Coated OTH Gown Yellow, Elastic Cuff, XX-Large, 10/bg

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

GMDN Terms

Code Name
35492 Isolation gown, single-use

Identifiers

Type ID
Package 10818566017519
Primary 00818566017512

Customer Contacts