FDA UDI In Commercial Distribution 🇺🇸 United States

OmniTrustTM

DI: 00810572006054 · Model: 9012-24 · OMNI INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
OmniTrustTM
Primary DI
00810572006054
Version / Model
9012-24
Catalog Number
9012-24
Company Name
OMNI INTERNATIONAL CORP.
Labeler DUNS
079434709
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2019-08-13
Public Version
1
Public Version Date
2019-08-21
Public Version Status
New
Public Device Record Key
f97c3b1f-f6e6-4800-b600-60495ae8bd9a

Device Description

Gauze Sponge, Non-Sterile, 2x2, 12 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
48133 Woven gauze pad, non-sterile

Identifiers

Type ID
Package 50810572006059
Primary 00810572006054
Unit of Use 10810572006051

Customer Contacts

Device Sizes

Type Value Unit Text
Width 2 Inch
Length 2 Inch