FDA UDI In Commercial Distribution 🇺🇸 United States

OmniTrustTM

DI: 00810572002612 · Model: 204-322 · OMNI INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
300

Basic Information

Brand Name
OmniTrustTM
Primary DI
00810572002612
Version / Model
204-322
Catalog Number
204-322
Company Name
OMNI INTERNATIONAL CORP.
Labeler DUNS
079434709
Distribution Status
In Commercial Distribution
Device Count in Pkg
300
Record Status
Published
Publish Date
2019-08-27
Public Version
3
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
58a82dc2-90f8-430c-a2e9-7472a8fb7db2

Device Description

Nitrile Examination Glove Powder Free Medium

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
No
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
LZA Polymer patient examination glove

GMDN Terms

Code Name
56286 Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Package 50810572002617
Primary 00810572002612
Unit of Use 10810572002619

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 40 Degrees Celsius