FDA UDI In Commercial Distribution 🇺🇸 United States

OmniTrustTM

DI: 00810572002162 · Model: 213-44 · OMNI INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
OmniTrustTM
Primary DI
00810572002162
Version / Model
213-44
Catalog Number
213-44
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
2020-06-19
Public Version Status
Update
Public Device Record Key
bfdada1d-b4ef-4926-909a-661816230082

Device Description

Nitrile Examination Glove Powder Free X-Large

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 50810572002167
Primary 00810572002162
Unit of Use 10810572002169

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 40 Degrees Celsius