Pure Global

SANSIN Hollow Fiber Haemodialysis Dialysers for Single Use - Indonesia BPOM Medical Device Registration

SANSIN Hollow Fiber Haemodialysis Dialysers for Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320561. The device is manufactured by JIANGXI SANXIN MEDTEC CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.

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 : C
SANSIN Hollow Fiber Haemodialysis Dialysers for Single Use
Analysis ID: AKL 20805320561

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. CEKINDO BUSINESS INTERNATIONAL

AR Address

CEKINDO BUSINESS INTERNATIONAL

Registration Date

Jan 25, 2023

Expiry Date

Oct 14, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing