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CDSCO UID IMP/IVD/2019/000135_e69000e43f72f7621aff934855f33536_418f62c4fb1e2a6c62ae86c6b9628f8a

Progesterone Assay

M/s. Ortho Clinical Diagnostics India Private Limited·Device Class Class B·India CDSCO·Brand: VITROS Immunodiagnostic Products Total T4 Reagent Pack
Registration details
UID
IMP/IVD/2019/000135_e69000e43f72f7621aff934855f33536_418f62c4fb1e2a6c62ae86c6b9628f8a
Device class
Class B
Brand name
VITROS Immunodiagnostic Products Total T4 Reagent Pack
License holder
M/s. Ortho Clinical Diagnostics India Private Limited
Approving authority
CDSCO
Product information
For in vitro diagnostic use only. For the quantitative measurement of progesterone in human serum and plasma (VITROS Immunodiagnostic Products Total T4 Reagent Pack) using the Immunodiagnostic Systems and the Integrated Systems
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About this record

Progesterone Assay is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000135_e69000e43f72f7621aff934855f33536_418f62c4fb1e2a6c62ae86c6b9628f8a. This device is marketed under the brand name VITROS Immunodiagnostic Products Total T4 Reagent Pack. The license holder is M/s. Ortho Clinical Diagnostics India Private Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.

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