Pure Global

REDAX Connectors - Indonesia BPOM Medical Device Registration

REDAX Connectors is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603816067. The device is manufactured by REDAX S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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 : B
REDAX Connectors
Analysis ID: AKL 21603816067

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

REDAX S.P.A.

Country of Origin

Italy

Authorized Representative

PT. IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

May 05, 2021

Expiry Date

Dec 02, 2025

Product Type

Surgical Equipment

Introduction/drainage catheter and accessories.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing