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REOCOR External Heart Pacemaker - Indonesia BPOM Medical Device Registration

REOCOR External Heart Pacemaker is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503515922. The device is manufactured by BIOTRONIK SE & CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : D. 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 : D
REOCOR External Heart Pacemaker
Analysis ID: AKL 30503515922

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Germany

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Aug 11, 2020

Expiry Date

Jan 28, 2025

Product Type

Prosthetic Cardiology Equipment

External pacemaker pulse generator.

Non Radiation Electromedics

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