ACCUTEST Drug Test Cup 12-Panel CLIA-Waived

GUDID 10763924822536

ACCUTEST Drug Test Cup 12-Panel CLIA-Waived AMP 1000, BAR 300, BZO 300, COC 300, MDMA 500, MAD 300, MET 1000, OPI 2000, OXY 100, PCP 25, TCA 1000 ,THC 50

JANT PHARMACAL CORPORATION

Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid Multiple drugs of abuse IVD, kit, rapid ICT, clinical Multiple drugs of abuse IVD, kit, rapid ICT, clinical Multiple drugs of abuse IVD, kit, rapid ICT, clinical Multiple drugs of abuse IVD, kit, rapid ICT, clinical Multiple drugs of abuse IVD, kit, rapid ICT, clinical Multiple drugs of abuse IVD, kit, rapid ICT, clinical

• Primary Device ID: 10763924822536
• NIH Device Record Key: 8f90e348-4cd5-425d-9fb2-277b9c30e79a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACCUTEST Drug Test Cup 12-Panel CLIA-Waived
• Version Model Number: DS822
• Company DUNS: 797393659
• Company Name: JANT PHARMACAL CORPORATION
• Device Count: 25
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00763924588539 [Unit of Use]
GS1	10763924822536 [Primary]

FDA Product Code

• LCM: Enzyme Immunoassay, Phencyclidine

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-05-24
• Device Publish Date: 2016-09-23

Devices Manufactured by JANT PHARMACAL CORPORATION

• 10763924851109 - Accustrip VALUE+ hCG Urine Pregnancy Test Strip (CLIA Waived): 2023-07-06 Accustrip VALUE+ hCG Urine Pregnancy Test Strip (CLIA Waived)
• 10763924853202 - Accutest VALUE+™ hCG Urine Pregnancy Test Cassette (CLIA Waived): 2023-07-06 Accutest VALUE+™ hCG Urine Pregnancy Test Cassette (CLIA Waived)
• 10763924864208 - Accutest VALUE+™ hCG Urine/Serum Pregnancy Test Cassette (CLIA-Waived for urine): 2023-07-06 Accutest VALUE+™ hCG Urine/Serum Pregnancy Test Cassette (CLIA-Waived for urine)
• 10763924095213 - Accutest Breath Alcohol Detector: 2022-11-28 Breath Alcohol Detector, .02 % BAC.
• 10763924097224 - Accustrip Saliva Alcohol Test: 2022-11-28 Saliva Alcohol Test Strip
• 10763924210142 - Accutest: 2022-11-28 2 Parameter Urine Reagent Strip (Glucose, Protein)
• 10763924410146 - Accutest: 2022-11-28 4-Parameter Urine Reagent Strip (Glucose, Protein, Nitrite, Leukocytes
• 10763924601568 - ACCUTEST Uriscreen Rapid Screen for UTI. Test: 2022-11-28 Rapid Screen for UTI, testing for Bacteriuria and presence of Somatic Cells in Urine.