FDA UDI In Commercial Distribution 🇺🇸 United States

OmniTrustTM

DI: 00810572006160 · Model: 9021-24 · OMNI INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
OmniTrustTM
Primary DI
00810572006160
Version / Model
9021-24
Catalog Number
9021-24
Company Name
OMNI INTERNATIONAL CORP.
Labeler DUNS
079434709
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2019-08-27
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
838d4c25-d5d0-403f-9d10-18303217a8e1

Device Description

Gauze Pads, 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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48134 Woven gauze pad

Identifiers

Type ID
Package 50810572006165
Primary 00810572006160
Unit of Use 10810572006167

Customer Contacts

Device Sizes

Type Value Unit Text
Width 2 Inch
Length 2 Inch