FDA UDI In Commercial Distribution 🇺🇸 United States

OmniTrustTM

DI: 00810572000397 · Model: 9112-31 · OMNI INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

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
OmniTrustTM
Primary DI
00810572000397
Version / Model
9112-31
Catalog Number
9112-31
Company Name
OMNI INTERNATIONAL CORP.
Labeler DUNS
079434709
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2020-12-10
Public Version
1
Public Version Date
2020-12-18
Public Version Status
New
Public Device Record Key
f580191a-b849-477b-a25c-802566d4993a

Device Description

Surgical Mask, Level 3, Earloop, Blue

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FXX Mask, Surgical

GMDN Terms

Code Name
35177 Surgical/medical face mask, single-use

Identifiers

Type ID
Package 50810572000392
Primary 00810572000397
Unit of Use 10810572000394

Customer Contacts

Phone
16034711499

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 40 Degrees Celsius