FDA UDI In Commercial Distribution 🇺🇸 United States

OmniTrustTM

DI: 00810572006566 · Model: 9101-42 · OMNI INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

Basic Information

Brand Name
OmniTrustTM
Primary DI
00810572006566
Version / Model
9101-42
Catalog Number
9101-41
Company Name
OMNI INTERNATIONAL CORP.
Labeler DUNS
079434709
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
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
63123f74-69b5-4394-9a33-477ea640a740

Device Description

Drain Sponge, Sterile, 4x4, 6 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
48131 Non-woven gauze pad

Identifiers

Type ID
Package 50810572006561
Primary 00810572006566
Unit of Use 10810572006563

Customer Contacts

Device Sizes

Type Value Unit Text
Length 4 Inch
Width 4 Inch