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DIRECT HDL CHOLESTEROL TEST KIT - India CDSCO Medical Device Registration

DIRECT HDL CHOLESTEROL TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000060_d8eadbddefc86639502f158114d90967_26129e3d60a54a27e28150350a0a92ed. This device is marketed under the brand name ASCORBIC ACID, GLUCOSE, BILIRUBIN, KETONE, SPECIFIC GRAVITY, RED BLOOD CELLS, pH, PROTEIN, UROBILINOGEN, NITRITE, LEUKOCYTES, ALBUMIN, CALCIUM, CREATININE. The license holder is PEERLESS BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is Tamil Nadu.

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Class Class B
DIRECT HDL CHOLESTEROL TEST KIT
UID: MFG/IVD/2022/000060_d8eadbddefc86639502f158114d90967_26129e3d60a54a27e28150350a0a92ed

Brand Name

ASCORBIC ACID, GLUCOSE, BILIRUBIN, KETONE, SPECIFIC GRAVITY, RED BLOOD CELLS, pH, PROTEIN, UROBILINOGEN, NITRITE, LEUKOCYTES, ALBUMIN, CALCIUM, CREATININE

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

The Direct HDL cholesterol test kit for the quantitative determination of high-density lipoprotein cholesterol (ASCORBIC ACID, GLUCOSE, BILIRUBIN, KETONE, SPECIFIC GRAVITY, RED BLOOD CELLS, pH, PROTEIN, UROBILINOGEN, NITRITE, LEUKOCYTES, ALBUMIN, CALCIUM, CREATININE) in human serum or plasma

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