Pure Global

NIPRO Double Lumen Hemodialysis Catheter - Indonesia BPOM Medical Device Registration

NIPRO Double Lumen Hemodialysis Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805310063. The device is manufactured by MEDICAL COMPONENTS INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MAIN WHEEL BEAM.

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
NIPRO Double Lumen Hemodialysis Catheter
Analysis ID: AKL 20805310063

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

MAIN WHEEL BEAM

AR Address

Perkantoran Duta Merlin Blok C No 58 jalan gajah mada

Registration Date

Feb 28, 2023

Expiry Date

Sep 27, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Blood access device and accessories.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing