Pure Global

GE Vaporizer - Indonesia BPOM Medical Device Registration

GE Vaporizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403810060. The device is manufactured by DATEX-OHMEDA, INC. USA from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GE OPERATIONS 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 : C
GE Vaporizer
Analysis ID: AKL 20403810060

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lantai 18-19 Jl. R.A. Kartini, Kav. 8 Kel. Cilandak Barat, Kec. Cilandak Jakarta Selataran 12430

Registration Date

Apr 13, 2022

Expiry Date

May 26, 2025

Product Type

Therapeutic Anesthesia Equipment

Anesthetic vaporizer.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from DATEX-OHMEDA, INC. USA
Products from the same manufacturer (1 products)