Pure Global

SAS Hollow Fiber Dialyzer - Indonesia BPOM Medical Device Registration

SAS Hollow Fiber Dialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220239. The device is manufactured by WEGO HEALTHCARE (SHENZHEN) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SING AJI SENTOSA.

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
SAS Hollow Fiber Dialyzer
Analysis ID: AKL 20805220239

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SING AJI SENTOSA

AR Address

Jl. Raya Pondok Gede No. 3 Pinang Ranti, Makassar, Jakarta Timur

Registration Date

Aug 11, 2022

Expiry Date

Aug 08, 2025

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
Other Products from WEGO HEALTHCARE (SHENZHEN) CO., LTD.
Products from the same manufacturer (1 products)