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AIKANG CK-MB In Vitro Diagnostic Kit (CK-MB) - Indonesia BPOM Medical Device Registration

AIKANG CK-MB In Vitro Diagnostic Kit (CK-MB) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101222267. The device is manufactured by AIKANG DIAGNOSTICS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOGEN SCIENTIFIC.

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BPOM Registered
Risk Class Kelas Resiko : B
AIKANG CK-MB In Vitro Diagnostic Kit (CK-MB)
Analysis ID: AKL 20101222267

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BIOGEN SCIENTIFIC

AR Address

Rukan Tanjung Mas Raya Jl.Raya Lenteng Agung Blok B1 No.21

Registration Date

Dec 19, 2022

Expiry Date

Jan 07, 2024

Product Type

Clinical Chemistry Test System

Creatine phosphokinase/creatine kinase or isoenzymes test system(kit & cair)

Invitro Diagnostics

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