BIOSET CK-MB LIQUIT - Indonesia BPOM Medical Device Registration
BIOSET CK-MB LIQUIT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221033. The device is manufactured by SCIENTIFIC MEDICAL PRODUCTS PAZ.SAN.VE TฤฐC. LTD.. STI from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDOPHARM NUSANTARA BIOMEDICINE.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Turkey
Authorized Representative
INDOPHARM NUSANTARA BIOMEDICINEAR Address
Jalan Griya Agung Blok O No.72,
Registration Date
Jul 15, 2022
Expiry Date
Dec 31, 2026
Product Type
Clinical Chemistry Test System
Creatine phosphokinase/creatine kinase or isoenzymes test system(kit & cair)
Invitro Diagnostics
