Aware Breast Self-Exam Pad

GUDID 00083059012033

Breast self-examination pad

Primary Device ID	00083059012033
NIH Device Record Key	b1a0029a-3526-4067-bfae-b6700b21013b
Commercial Distribution Status	In Commercial Distribution
Brand Name	Aware Breast Self-Exam Pad
Version Model Number	1203
Company DUNS	067647321
Company Name	BIOMERICA, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	true
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00083059012033 [Primary]

IYO	System, Imaging, Pulsed Echo, Ultrasonic

Steralize Prior To Use	false
Device Is Sterile	false

00083059012071	The Aware™ Pad is intended to be used as an aid for performing breast self-examination.
00083059012033	The Aware™ Pad is intended to be used as an aid for performing breast self-examination.
08305900012033	The Aware™ Pad is intended to be used as an aid for performing breast self-examination.