FDA UDI In Commercial Distribution 🇺🇸 United States

Aware Breast Self-Exam Pad

DI: 00083059012033 · Model: 1203 · BIOMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aware Breast Self-Exam Pad
Primary DI
00083059012033
Version / Model
1203
Company Name
BIOMERICA, INC.
Labeler DUNS
067647321
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-01
Public Version
1
Public Version Date
2020-07-09
Public Version Status
New
Public Device Record Key
b1a0029a-3526-4067-bfae-b6700b21013b

Device Description

The Aware™ Pad is intended to be used as an aid for performing breast self-examination.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYO System, Imaging, Pulsed Echo, Ultrasonic

GMDN Terms

Code Name
44007 Breast self-examination pad

Identifiers

Type ID
Primary 00083059012033

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K991469 000