Pure Global

SUMI Tracheostomy Tube without Cuff, Siliconised - Indonesia BPOM Medical Device Registration

SUMI Tracheostomy Tube without Cuff, Siliconised is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403024879. The device is manufactured by SUMI SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ SP, K. from Poland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.

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
SUMI Tracheostomy Tube without Cuff, Siliconised
Analysis ID: AKL 20403024879

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Poland

Authorized Representative

PT. SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

Dec 12, 2022

Expiry Date

Nov 04, 2025

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