DEVICE: ACCUTEST Drug Test Cup 13-Panel CLIA-Waived (10763924823533)
Device Identifier (DI) Information
ACCUTEST Drug Test Cup 13-Panel CLIA-Waived
DS823
In Commercial Distribution
JANT PHARMACAL CORPORATION
DS823
In Commercial Distribution
JANT PHARMACAL CORPORATION
ACCUTEST Drug Test Cup 13-Panel CLIA-Waived
AMP 1000, BAR 300, BZO 300, BUP 10, COC 300, MDMA 500, MAD 300, MET 1000, OPI 300, OXY 100, PCP 25, TCA 1000, THC 50
Device Characteristics
Labeling does not contain MRI Safety Information | |
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No | |
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No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
46994 | Multiple drugs of abuse IVD, kit, rapid ICT, clinical |
A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of multiple drugs of abuse in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
LCM | Enzyme Immunoassay, Phencyclidine |
LFH | U.V. Spectrometry, Tricyclic Antidepressant Drugs |
LDJ | Enzyme Immunoassay, Cannabinoids |
DJR | Enzyme Immunoassay, Methadone |
DJC | Thin Layer Chromatography, Methamphetamine |
DIO | Enzyme Immunoassay, Cocaine And Cocaine Metabolites |
JXM | Enzyme Immunoassay, Benzodiazepine |
DIS | Enzyme Immunoassay, Barbiturate |
DKZ | Enzyme Immunoassay, Amphetamine |
DJG | Enzyme Immunoassay, Opiates |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
4e74aad7-ffd9-438b-81be-5c3bbb1d3a94
June 10, 2022
4
September 23, 2016
June 10, 2022
4
September 23, 2016
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
00763924822539
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined