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GREINER Creatin Kinase-MB - Indonesia BPOM Medical Device Registration

GREINER Creatin Kinase-MB is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101815545. The device is manufactured by GREINER DIAGNOSTIC GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RAJAWALI NUSINDO.

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
GREINER Creatin Kinase-MB
Analysis ID: AKL 20101815545

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. RAJAWALI NUSINDO

AR Address

Gedung RNI Jl. Denpasar Raya Kav DIII Kuningan Jakarta Selatan

Registration Date

Jan 06, 2022

Expiry Date

Nov 11, 2026

Product Type

Clinical Chemistry Test System

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

Invitro Diagnostics

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