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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 20902322844. 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 TRIMEDIK SURYA SELARAS.

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
COMEN Infusion Pump
Analysis ID: AKL 20902322844

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

TRIMEDIK SURYA SELARAS

AR Address

JL MH Thamrin Kebon Nanas, Duta Incah Iconic Blok B No 1 RT006/002,Panunggangan utara,pinang,jota tangerang Banten.

Registration Date

Nov 15, 2023

Expiry Date

Aug 22, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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