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GENMED Oxygen Regulator - Indonesia BPOM Medical Device Registration

GENMED Oxygen Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402320128. 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. MEGA KREASI ALKESINDO.

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
GENMED Oxygen Regulator
Analysis ID: AKL 10402320128

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. MEGA KREASI ALKESINDO

AR Address

MEGA KREASI ALKESINDO

Registration Date

Oct 30, 2023

Expiry Date

Oct 29, 2026

Product Type

Monitoring Anesthesia Equipment

Pressure regulator.

Non Electromedic Non Sterile

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