10,000 results
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51ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AIMSCREEN BZO
FDA UDI
GERMAINE LABORATORIES, INC·00695684423254·Lateral flow immunoassay for the detection of B...
ACCUSIGN BZO, BIOSIGN BZO, STATUS BZO
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ImmuTest Drugs of Abuse Screen Card
FDA UDI
AMEDITECH INC.·00816565020021·Benzodiazepine single drug dipcard
AccuSign® BZO card
FDA UDI
PRINCETON BIOMEDITECH CORPORATION·10743816000167·AccuSign® BZO card; 35 Test kit; CE
BZO Rapid Test Cassette
FDA UDI
ACRO BIOTECH INC·00853691007120·BZO Rapid Test Cassette
AccuSign® BZO card
FDA UDI
PRINCETON BIOMEDITECH CORPORATION·10743816000174·AccuSign® BZO card; 10 Test kit; CE
ACCUSIGN DOA3, DOA3(BZO/BAR/PCP), BZO/BAR/PCP, BIOSIGN DOA3, DOA3(BZO/BAR/PCP), BZO/BAR/PCP
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ACCUSIGN DOA2, DOA, BAR/BZO, BIOSIGN DOA2, BAR/BZO, STATUS DS BAR/BZO, SYVA RAPIDTEST D.A.U. 2 BAR/BZO
FDA 510(k)
FDA Class 2
·Clinical Toxicology
UCP Home Drug Screening Test Cards
FDA UDI
UCP BIOSCIENCES, INC.·10817038021498·UCP Home Drug Screening Test Cards BZO Single P...
Rapid Response
FDA UDI
BTNX Inc·00722066000502·Rapid Response Single Drug Test Strips (BZO) - ...
UCP Home
FDA UDI
UCP BIOSCIENCES, INC.·10817038021245·UCP Home Drug Screening Test Strips
Benzodiaze...
Alere iScreen Dx
FDA UDI
Instant Technologies, Inc.·00817405020065·Urine Drug Screen Card for detection of Benzodi...
Precision DX
FDA UDI
AMERICAN SCREENING, L.L.C.·00840050510735·
Rapid Response
FDA UDI
BTNX Inc·00722066000519·Rapid Response Single Drug Test Cassettes (BZO)...
Precision DX
FDA UDI
AMERICAN SCREENING, L.L.C.·00840050510742·
UCP Home Drug Screening Test Cards
FDA UDI
UCP BIOSCIENCES, INC.·10817038020439·BZO Single Panel Dip Test Card
u-Card
FDA UDI
UCP BIOSCIENCES, INC.·10817038021405·u-Card BZO Single Panel Dip Test Card
ACCUSIGN DOA 3/DOA 3 (BZO/BAR/PCP), BZO/BAR/PCP, BIOSIGN DOA 3/BZO/BAR/PCP, BIOSIGN BZO/BAR/PCP
FDA 510(k)
FDA Class 2
·Clinical Toxicology
(COC/AMP/EDDP100/MOP/BZO)MULTI-DRUG ONE STEP 5 DRUG SCREEN TEST PANEL (URINE)
FDA Adverse Event
Malfunction
·Product code DIO·December 10, 2015
VERDICT -II BAR/BZO
FDA 510(k)
FDA Class 2
·Clinical Toxicology