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DAY Hemodialyzer - Indonesia BPOM Medical Device Registration

DAY Hemodialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220401. The device is manufactured by DIALIFE SA from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRAHA KREASI MEDIKA.

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
DAY Hemodialyzer

DIA Hemodialyzer

Analysis ID: AKL 20805220401

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

DIALIFE SA

Country of Origin

Switzerland

Authorized Representative

PT. GRAHA KREASI MEDIKA

AR Address

Pakuwon Tower Kota Kasablanka Lt. 10 Unit J, Jl.Casablanca No. 88

Registration Date

Nov 03, 2022

Expiry Date

Oct 31, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

High permeability hemodialysis system.

Non Radiation Electromedics

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