Pure Global

ONECARE Medical Oxygen Regulator - Indonesia BPOM Medical Device Registration

ONECARE Medical Oxygen Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402124315. The device is manufactured by YUYAO YUFENG MEDICAL EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. CENTRAL MEDIKA 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 : A
ONECARE Medical Oxygen Regulator
Analysis ID: AKL 10402124315

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. CENTRAL MEDIKA INDONESIA

AR Address

Jl. Candi Mutiara Selatan III/ 317 RT.03/06 Kalipancur

Registration Date

Jul 11, 2024

Expiry Date

Jul 11, 2027

Product Type

Monitoring Anesthesia Equipment

Pressure regulator.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing