Pure Global

HONG AN Endotracheal Tube - Indonesia BPOM Medical Device Registration

HONG AN Endotracheal Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403813746. The device is manufactured by NANJING HONG AN MEDICAL APPLIANCE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALEXA MEDIKA.

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
HONG AN Endotracheal Tube
Analysis ID: AKL 20403813746

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ALEXA MEDIKA

AR Address

Jl. Yos Sudarso Komplek Graha Niaga Blok C No. 14

Registration Date

Dec 01, 2020

Expiry Date

Sep 01, 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
Other Products from NANJING HONG AN MEDICAL APPLIANCE CO., LTD.
Products from the same manufacturer (1 products)