Pure Global

DRAEGER Patient Monitor - Indonesia BPOM Medical Device Registration

DRAEGER Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502714778. The device is manufactured by DRAEGERWERK AG & CO., KGAA. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DRAEGER MEDICAL 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
DRAEGER Patient Monitor
Analysis ID: AKL 20502714778

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

DRAEGER MEDICAL INDONESIA

AR Address

ALAMANDA TOWER Lt. 32 Unit A,B,D,E,F. Jl. TB. Simatupang Kav. 23-24

Registration Date

Nov 03, 2023

Expiry Date

Jul 14, 2027

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing