Pure Global

DIALIFE Biocart DLC-650 - Indonesia BPOM Medical Device Registration

DIALIFE Biocart DLC-650 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220452. The device is manufactured by INSPRAMED MEDICAL SAN TIC. A.S. from Turkey, 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
DIALIFE Biocart DLC-650
Analysis ID: AKL 20805220452

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. GRAHA KREASI MEDIKA

AR Address

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

Registration Date

Nov 25, 2022

Expiry Date

Oct 31, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing