FDA UDI In Commercial Distribution 🇺🇸 United States

OmniTrustTM

DI: 00810572006382 · Model: 9083-22 · OMNI INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
OmniTrustTM
Primary DI
00810572006382
Version / Model
9083-22
Catalog Number
9083-22
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
1
Public Version Date
2019-09-04
Public Version Status
New
Public Device Record Key
6f114084-1be2-4460-bf1b-5c673976e9ba

Device Description

Adhesive Bandages, sheer, 1x3

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KGX Tape and bandage, adhesive

GMDN Terms

Code Name
34864 Adhesive bandage

Identifiers

Type ID
Package 50810572006387
Primary 00810572006382
Unit of Use 10810572006389

Customer Contacts

Device Sizes

Type Value Unit Text
Length 1 Inch
Width 3 Inch