FDA UDI In Commercial Distribution 🇺🇸 United States

OmniTrustTM

DI: 00810572000861 · Model: 313-11 · OMNI INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
150

Basic Information

Brand Name
OmniTrustTM
Primary DI
00810572000861
Version / Model
313-11
Catalog Number
313-11
Company Name
OMNI INTERNATIONAL CORP.
Labeler DUNS
079434709
Distribution Status
In Commercial Distribution
Device Count in Pkg
150
Record Status
Published
Publish Date
2019-09-06
Public Version
1
Public Version Date
2019-09-16
Public Version Status
New
Public Device Record Key
50aa55be-7b7c-47d1-aa72-061f2b4c4b53

Device Description

Vinyl Examination Glove Powder Free Small

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
LYZ Vinyl patient examination glove

GMDN Terms

Code Name
47176 Vinyl examination/treatment glove, non-powdered

Identifiers

Type ID
Package 50810572000866
Primary 00810572000861
Unit of Use 10810572000868

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-10 – 40 Degrees Celsius