FDA UDI In Commercial Distribution 🇺🇸 United States

OmniTrust

DI: 00810572002247 · Model: 315-14 · OMNI INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
OmniTrust
Primary DI
00810572002247
Version / Model
315-14
Catalog Number
315-14
Company Name
OMNI INTERNATIONAL CORP.
Labeler DUNS
079434709
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2025-05-15
Public Version
1
Public Version Date
2025-05-23
Public Version Status
New
Public Device Record Key
59bf6d29-4c22-4794-bf47-6de5d8583f9c

Device Description

OmniTrust Vinyl Examination Gloves, 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
LYZ Vinyl Patient Examination Glove

GMDN Terms

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

Identifiers

Type ID
Package 50810572002242
Primary 00810572002247
Unit of Use 10810572002244

Customer Contacts

Phone
6034711499

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 40 Degrees Celsius