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MEDIPLUS Hemodialysis Catheter Kit - Indonesia BPOM Medical Device Registration

MEDIPLUS Hemodialysis Catheter Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805520009. The device is manufactured by SHREE UMIYA SURGICAL PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAGENTA BIOMEDIKA.

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
MEDIPLUS Hemodialysis Catheter Kit
Analysis ID: AKL 20805520009

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. MAGENTA BIOMEDIKA

AR Address

Ruko Buaran Persada No. 30, Jl. Raya Soekamto, Duren Sawit

Registration Date

Jan 13, 2025

Expiry Date

Jun 01, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Blood access device and accessories.

Non Electromedic Sterile

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