Pure Global

COMEN Infusion Pump - Indonesia BPOM Medical Device Registration

COMEN Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420799. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENTS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
COMEN Infusion Pump
Analysis ID: AKL 20902420799

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

COMEN BIOMEDICAL INDONESIA

AR Address

Citra 8, Aerobliss Blok C2E Nomor 10

Registration Date

Aug 04, 2024

Expiry Date

Apr 29, 2029

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing