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CDSCO UID IMP/IVD/2022/000035_e3664b64baf174194ef86821c9a3cb98_9be6280aab63bde21ed61ae73b85c4bb

FT4 Rapid Quantitative Test

DIYA SCIENTIFIC·Device Class Class B·India CDSCO·Brand: Immunoglobulin E
Registration details
UID
IMP/IVD/2022/000035_e3664b64baf174194ef86821c9a3cb98_9be6280aab63bde21ed61ae73b85c4bb
Device class
Class B
Brand name
Immunoglobulin E
License holder
DIYA SCIENTIFIC
Approving authority
CDSCO
Product information
The Biotime FT4 Rapid Quantitative Test is intended to quantify the concentration of FT4 in human serum on Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an aid detection of hyperthyroidism. -Fluorescence immunoassay -hyperthyroidism For in vitro diagnostic use only. For professional use only.
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HbA1c Rapid Quantitative Test-It is intended to quantify the percentage of HbA1c in human whole blood on Biotime FIA Analyzer by fluorescent immunoassay.The test is used as an aid in management and monitoring of the long-term glycemic status in patients with diabetes mellitus.,β-hCG Rapid Quantitative Test
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About this record

FT4 Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000035_e3664b64baf174194ef86821c9a3cb98_9be6280aab63bde21ed61ae73b85c4bb. This device is marketed under the brand name Immunoglobulin E. The license holder is DIYA SCIENTIFIC, and it is classified as Device Class Class B. The approving authority is CDSCO.

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