Pure Global

Portex BLUperc Percutaneous Dilation Tracheostomy Kit - Indonesia BPOM Medical Device Registration

Portex BLUperc Percutaneous Dilation Tracheostomy Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420031. The device is manufactured by SMITHS MEDICAL CZECH REPUBLIC A.S from Czech Republic, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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
Portex BLUperc Percutaneous Dilation Tracheostomy Kit
Analysis ID: AKL 20403420031

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Czech Republic

Authorized Representative

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

Feb 01, 2025

Expiry Date

Nov 22, 2029

Product Type

Therapeutic Anesthesia Equipment

Tracheostomy tube and tube cuff.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing