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ONEMED Medical Oxygen Regulator - Indonesia BPOM Medical Device Registration

ONEMED Medical Oxygen Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402220037. The device is manufactured by NINGBO KAIPO ELECTRON INSTRUMENT AND METER CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INTIGLOBAL PERFECT RESULT SOURCE.

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 : A
ONEMED Medical Oxygen Regulator
Analysis ID: AKL 10402220037

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. INTIGLOBAL PERFECT RESULT SOURCE

AR Address

KOMPLEK DARMO PARK II BLOK 4/14

Registration Date

Jun 21, 2022

Expiry Date

Jun 19, 2025

Product Type

Monitoring Anesthesia Equipment

Pressure regulator.

Non Radiation Electromedics

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