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SINOCARE Myocardial Enzyme Reagent Kit - Indonesia BPOM Medical Device Registration

SINOCARE Myocardial Enzyme Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101126314. The device is manufactured by CHANGSHA SINOCARE INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SINOCARE HEALTHCARE INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
SINOCARE Myocardial Enzyme Reagent Kit
Analysis ID: AKL 20101126314

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SINOCARE HEALTHCARE INDONESIA

AR Address

Equity Tower Lantai 37, SCBD, Jl.Jend. Sudirman Kav.52-53

Registration Date

Dec 02, 2023

Expiry Date

Sep 13, 2026

Product Type

Clinical Chemistry Test System

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

Invitro Diagnostics

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