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BROSMEDIC Hollow Fiber Dialyzer - Indonesia BPOM Medical Device Registration

BROSMEDIC Hollow Fiber Dialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805122422. The device is manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BARAKAH MEDIKA NUSANTARA.

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
BROSMEDIC Hollow Fiber Dialyzer
Analysis ID: AKL 20805122422

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BARAKAH MEDIKA NUSANTARA

AR Address

Jl. veteran no. 48 Bekasi 17141

Registration Date

May 06, 2021

Expiry Date

Apr 28, 2024

Product Type

Therapeutic Gastroenterology-Urology Equipment

High permeability hemodialysis system.

Non Electromedic Sterile

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