Primary Device ID | 00083059100013 |
NIH Device Record Key | ec47ca5f-6b24-4efb-931c-abe2886639fa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EZ Detect Colon Disease Test |
Version Model Number | 1000-1 |
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 | true |
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 | true |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com | |
Phone | +1 949 645 2111 |
info@biomerica.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00083059100013 [Primary] |
KHE | Reagent, Occult Blood |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-09 |
Device Publish Date | 2020-07-01 |
00083059100013 | Home Test For Hidden Blood in The Stool |
08305900100013 | Home Test For Hidden Blood in The Stool |