Primary Device ID | 06977469280042 |
NIH Device Record Key | cb022133-c857-4793-9351-13b2acd8682e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | U-Catch PLUS Multi-Drug Test Cup Cup(Colloidal Gold) |
Version Model Number | ETG004025 |
Company DUNS | 638595825 |
Company Name | Eterbio, 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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06977469280042 [Primary] |
NFV | Test, Benzodiazepine, Over The Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-25 |
Device Publish Date | 2024-12-17 |
06977469280042 | 25 Tests/Kit;12 Panel;AMP;BAR;BUP;BZO;COC;MDMA;MET;MOP;MTD;OXY;PCP;THC;CR;PH;SG |
06977469280011 | 1 Test/Kit;12 Panel;AMP,BAR,BUP,BZO,COC,MDMA,MET,MOP,MTD,OXY,PCP,THC |