FDA UDI In Commercial Distribution 🇺🇸 United States

OmniTrustTM

DI: 00810572001530 · Model: 214-22 · OMNI INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
OmniTrustTM
Primary DI
00810572001530
Version / Model
214-22
Catalog Number
214-22
Company Name
OMNI INTERNATIONAL CORP.
Labeler DUNS
079434709
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2019-08-27
Public Version
4
Public Version Date
2022-12-26
Public Version Status
Update
Public Device Record Key
aace72ba-ef81-43ac-b299-bad63d10b6d2

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 50810572001535
Primary 00810572001530
Unit of Use 10810572001537

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K131440 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 40 Degrees Celsius