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LDH SCE mod. liquiUV [HumaStar 300 SR, HumaStar 600] - India CDSCO Medical Device Registration

LDH SCE mod. liquiUV [HumaStar 300 SR, HumaStar 600] is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_cc57ff3194198280c07782abb152ac0a_dce38f740f865ad66eb5db3fa00fb4bb. The license holder is Stedman Pharmaceuticals Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered
Class Class B
LDH SCE mod. liquiUV [HumaStar 300 SR, HumaStar 600]
UID: IMP/IVD/2019/000206_cc57ff3194198280c07782abb152ac0a_dce38f740f865ad66eb5db3fa00fb4bb

Device Class

Class B

Approving Authority

CDSCO

Product Information

Enzymatic UV test for the quantitative determination of lactate dehydrogenase ##PLACEHOLDER_0## in human serum and plasma on HumaStar 300 SR and HumaStar 600

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