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BIOMONITOR III - Indonesia BPOM Medical Device Registration

BIOMONITOR III is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501028031. The device is manufactured by BIOTRONIC SE & CO. KG from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.

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 : C
BIOMONITOR III
Analysis ID: AKL 20501028031

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Dec 21, 2020

Expiry Date

Jun 02, 2025

Product Type

Diagnostic Cardiology Equipment

Arrhythmia detector and alarm (including ST-segment measurement and alarm).

Non Radiation Electromedics

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