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OXYVAC Flowmeter Oxygen - Indonesia BPOM Medical Device Registration

OXYVAC Flowmeter Oxygen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402320088. The device is manufactured by OXYVAC MEDICAL INSTRUMENT CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SURICON SCINTILLATING WORKS.

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
OXYVAC Flowmeter Oxygen
Analysis ID: AKL 10402320088

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

SURICON SCINTILLATING WORKS

AR Address

Wonorejo Selatan,Perum Amerta B-1)

Registration Date

May 07, 2023

Expiry Date

Mar 05, 2025

Product Type

Monitoring Anesthesia Equipment

Pressure regulator.

Non Electromedic Non Sterile

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