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BRAUN Anaesthesia System - Indonesia BPOM Medical Device Registration

BRAUN Anaesthesia System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403213146. The device is manufactured by BRAUN AND COMPANY LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GLOBAL SYSTECH 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.

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BPOM Registered
Risk Class Kelas Resiko : C
BRAUN Anaesthesia System
Analysis ID: AKL 20403213146

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. GLOBAL SYSTECH MEDIKA

AR Address

Jl. TB Simatupang No.17 RT.011/002 Kel. Susukan, Kec. Ciracas Jakarta Timur

Registration Date

May 29, 2023

Expiry Date

Apr 19, 2025

Product Type

Therapeutic Anesthesia Equipment

Gas machine for anesthesia or analgesia.

Non Radiation Electromedics

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