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CDSCO UID IMP/IVD/2019/000206_cc57ff3194198280c07782abb152ac0a_dce38f740f865ad66eb5db3fa00fb4bb

LDH SCE mod. liquiUV [HumaStar 300 SR, HumaStar 600]

Stedman Pharmaceuticals Pvt. Ltd.·Device Class Class B·India CDSCO
Registration details
UID
IMP/IVD/2019/000206_cc57ff3194198280c07782abb152ac0a_dce38f740f865ad66eb5db3fa00fb4bb
Device class
Class B
License holder
Stedman Pharmaceuticals Pvt. Ltd.
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
Other products from Stedman Pharmaceuticals Pvt. Ltd.
Products from the same license holder (10 products)
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URIC ACID liquicolor plus
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SODIUM liquicolor [HumaStar 300SR, HumaStar 600]
Class B
HC5D DIFF LYSE
Class B
MAGNESIUM liquicolor
Class B
HDL CHOLESTEROL liquicolor [HumaStar 300SR, HumaStar 600]
Class B
About this record

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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