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AIM CK-MB Q Rapid Test - Indonesia BPOM Medical Device Registration

AIM CK-MB Q Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221156. The device is manufactured by VEDA LAB from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ACCURATE INTAN MADYA.

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
AIM CK-MB Q Rapid Test
Analysis ID: AKL 20101221156

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

VEDA LAB

Country of Origin

France

Authorized Representative

PT. ACCURATE INTAN MADYA

AR Address

Komplek Duta Merlin Blok F No.5-6. Jl.Gajah Mada No.3-5

Registration Date

Aug 15, 2022

Expiry Date

Aug 03, 2025

Product Type

Clinical Chemistry Test System

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

Invitro Diagnostics

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