KEMILO CK-MB Kit - Indonesia BPOM Medical Device Registration
KEMILO CK-MB Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221715. The device is manufactured by GOLDSITE DIAGNOSTICS INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SUMIFIN CITRA ABADI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GOLDSITE DIAGNOSTICS INC.Country of Origin
China
Authorized Representative
PT. SUMIFIN CITRA ABADIAR Address
Jl. Alam Sutera Boulevard Alam Sutera Town Center (ASTC) Blok 10D No.19, Kel. Pakulonan, Kec. Serpong Utara - Tangerang Selatan 15325
Registration Date
Oct 13, 2022
Expiry Date
May 15, 2025
Product Type
Clinical Chemistry Test System
Creatine phosphokinase/creatine kinase or isoenzymes test system(kit & cair)
Invitro Diagnostics
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GOLDSITE GPP 100 Protein Analyzer
GOLDSITE Anti-CCP Control Level 3
GOLDSITE Multiple Control
GOLDSITE HbA1c Control H
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