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COMEN Semi-Automated External - Indonesia BPOM Medical Device Registration

COMEN Semi-Automated External is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505420123. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENTS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is COMEN BIOMEDICAL 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 : D
COMEN Semi-Automated External
Analysis ID: AKL 30505420123

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

COMEN BIOMEDICAL INDONESIA

AR Address

Citra 8, Aerobliss Blok C2E Nomor 10

Registration Date

Oct 02, 2024

Expiry Date

Apr 29, 2029

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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