| Primary Device ID | 08305900010015 |
| NIH Device Record Key | caf07d6b-c8b8-431b-a27e-c5a5a05f9c11 |
| Commercial Distribution Discontinuation | 2020-07-01 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | EZ Detect Fecal Occult Blood Test |
| Version Model Number | 1001 |
| 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 |
| 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 | 08305900010015 [Primary] |
| KHE | Reagent, Occult Blood |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2021-09-02 |
| Device Publish Date | 2016-12-08 |
| 00083059010015 | The EZ DETECT Test is for in vitro qualitative detection of occult blood in the stool -- an earl |
| 08305900010015 | The EZ DETECT Test is for in vitro qualitative detection of occult blood in the stool -- an earl |