ICHROMA™ CK-MB - Indonesia BPOM Medical Device Registration
ICHROMA™ CK-MB is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101324242. The device is manufactured by BODITECH WITH INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ZOE PELITA NUSANTARA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BODITECH WITH INC.Country of Origin
Korea
Authorized Representative
PT. ZOE PELITA NUSANTARAAR Address
JALAN CIKINI II NO 8 B
Registration Date
Nov 13, 2023
Expiry Date
Oct 01, 2027
Product Type
Clinical Chemistry Test System
Creatine phosphokinase/creatine kinase or isoenzymes test system (card)
Invitro Diagnostics
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