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ALKALINE PHOSPHATASE Test Reagent - India CDSCO Medical Device Registration

ALKALINE PHOSPHATASE Test Reagent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000036_c6daaaefe734c436169df56a8e609baf_d9055d0c9abec4ea4c2c26204e07df9b. This device is marketed under the brand name SEDONA. The license holder is M/s STEDMAN PHARMACEUTICALS PVT. LTD., and it is classified as Device Class Class B. The approving authority is Tamil Nadu.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
ALKALINE PHOSPHATASE Test Reagent
UID: MFG/IVD/2019/000036_c6daaaefe734c436169df56a8e609baf_d9055d0c9abec4ea4c2c26204e07df9b

Brand Name

SEDONA

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

Diagnostic reagent is intended for in vitro quantitative determination of ALP in human serum and plasma

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