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HiCiCHA Hollow Fiber Dialyzer P-Series (Mid-Low Flux) - Indonesia BPOM Medical Device Registration

HiCiCHA Hollow Fiber Dialyzer P-Series (Mid-Low Flux) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220318. 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. HICLEARANCE MEDICAL 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 : C
HiCiCHA Hollow Fiber Dialyzer P-Series (Mid-Low Flux)
Analysis ID: AKL 20805220318

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. HICLEARANCE MEDICAL INDONESIA

AR Address

Kawasan Industri Cakung Cilincing, Jalan Cakung Industri Selatan 1 No. 12

Registration Date

Sep 13, 2022

Expiry Date

Sep 30, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

High permeability hemodialysis system.

Non Electromedic Sterile

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