Pure Global

HEMOFILTER - Indonesia BPOM Medical Device Registration

HEMOFILTER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420151. The device is manufactured by MEDICA S.P.A from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PRIMA CENTER MEDIKACITRA.

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
HEMOFILTER
Analysis ID: AKL 20805420151

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MEDICA S.P.A

Country of Origin

Italy

Authorized Representative

PRIMA CENTER MEDIKACITRA

AR Address

JL. PASEBAN RAYA NO.21

Registration Date

Mar 19, 2024

Expiry Date

Oct 26, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

High permeability hemodialysis system.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing