CDSCO UID IMP/IVD/2023/000502_e82f11ed94b39e8aa648d2099336865d_858201dcac21626328699815254d422d

COPPER

ARK Diagnostic System Pvt.Ltd·Device Class Class B·India CDSCO·Brand: QCA
Registration details
UID
IMP/IVD/2023/000502_e82f11ed94b39e8aa648d2099336865d_858201dcac21626328699815254d422d
Device class
Class B
Brand name
QCA
Approving authority
CDSCO
Product information
For “ in vitro” determination of copper in serum or plasma
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Products from the same license holder (10 products)
PROTEIN CONTROL
Brand: QCA
Class B
IMMUNOGLOBULIN A
Brand: QCA
Class B
TOTAL PROTEIN
Brand: QCA
Class B
CHOLINESTERASE
Brand: QCA
Class B
URIC ACID LIQUID
Brand: QCA
Class B
MICROALBUMIN
Brand: QCA
Class B
UREA ENZYMATIC
Brand: QCA
Class B
HEMOSCANN
Brand: QCA
Class B
UREA U.V
Brand: QCA
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AS DIRECT LATEX
Brand: QCA
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About this record

COPPER is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000502_e82f11ed94b39e8aa648d2099336865d_858201dcac21626328699815254d422d. This device is marketed under the brand name QCA. The license holder is ARK Diagnostic System Pvt.Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.

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