Pure Global

PURIFIER L180 Low Flux Dialyser - Indonesia BPOM Medical Device Registration

PURIFIER L180 Low Flux Dialyser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220130. The device is manufactured by SAFIL MEDICAL PRODUCTS INTERNATIONAL TRANSPORT INDUSTRY AND TRADE CO., LTD., from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is RENALMED TIARA MAIN.

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
PURIFIER L180 Low Flux Dialyser
Analysis ID: AKL 20805220130

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

RENALMED TIARA MAIN

AR Address

Gedung Enseval Lantai 2 Jl. Pulo Lentut No. 10 Kawasan Industri Pulogadung, Jakarta Timur Tlp. 021-4618330

Registration Date

May 16, 2022

Expiry Date

Jul 13, 2026

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 SAFIL MEDICAL PRODUCTS INTERNATIONAL TRANSPORT INDUSTRY AND TRADE CO., LTD.,
Products from the same manufacturer (2 products)