EZ Detect Colon Disease Test

GUDID 00083059100013

Home Test For Hidden Blood in The Stool

BIOMERICA, INC.

Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, chromogenic, rapid Faecal occult blood IVD, kit, rapid colorimetric, clinical Faecal occult blood IVD, kit, rapid colorimetric, clinical Faecal occult blood IVD, kit, rapid colorimetric, clinical Faecal occult blood IVD, kit, rapid colorimetric, clinical Faecal occult blood IVD, kit, rapid colorimetric, clinical Faecal occult blood IVD, kit, rapid colorimetric, clinical Faecal occult blood IVD, kit, rapid colorimetric, clinical Faecal occult blood IVD, kit, rapid colorimetric, clinical Faecal occult blood IVD, kit, rapid colorimetric, clinical Faecal occult blood IVD, kit, rapid colorimetric, clinical Faecal occult blood IVD, kit, rapid colorimetric, clinical
Primary Device ID00083059100013
NIH Device Record Keyec47ca5f-6b24-4efb-931c-abe2886639fa
Commercial Distribution StatusIn Commercial Distribution
Brand NameEZ Detect Colon Disease Test
Version Model Number1000-1
Company DUNS067647321
Company NameBIOMERICA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com
Phone+1 949 645 2111
Emailinfo@biomerica.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100083059100013 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KHEReagent, Occult Blood

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-09
Device Publish Date2020-07-01

On-Brand Devices [EZ Detect Colon Disease Test]

00083059100013Home Test For Hidden Blood in The Stool
08305900100013Home Test For Hidden Blood in The Stool

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.