Pure Global

SHILEY™ Nasal RAE Tracheal Tube Cuffed / Murphy Eye - Indonesia BPOM Medical Device Registration

SHILEY™ Nasal RAE Tracheal Tube Cuffed / Murphy Eye is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403712963. The device is manufactured by MALLINCKRODT MEDICAL from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDTRONIC 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
SHILEY™ Nasal RAE Tracheal Tube Cuffed / Murphy Eye
Analysis ID: AKL 20403712963

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Ireland

Authorized Representative

MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Nov 23, 2020

Expiry Date

Oct 21, 2025

Product Type

Therapeutic Anesthesia Equipment

Tracheal tube.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing