FDA UDI In Commercial Distribution 🇺🇸 United States

OmniTrustTM

DI: 00810572006191 · Model: 9032-21 · OMNI INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
OmniTrustTM
Primary DI
00810572006191
Version / Model
9032-21
Catalog Number
9032-21
Company Name
OMNI INTERNATIONAL CORP.
Labeler DUNS
079434709
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2019-08-27
Public Version
1
Public Version Date
2019-09-04
Public Version Status
New
Public Device Record Key
475e4b9f-b1b5-418f-93db-0180b35f74b0

Device Description

Non-Woven Sponge, Non-Sterile, 2x2, 4 Ply

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
No
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
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48130 Non-woven gauze pad, non-sterile

Identifiers

Type ID
Package 50810572006196
Primary 00810572006191
Unit of Use 10810572006198

Customer Contacts

Device Sizes

Type Value Unit Text
Length 2 Inch
Width 2 Inch