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OXYWISE Oxygen Generator - Indonesia BPOM Medical Device Registration

OXYWISE Oxygen Generator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403915113. The device is manufactured by OXYWISE S.R.O from Slovakia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. OXY INDOMED.

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 : B
OXYWISE Oxygen Generator
Analysis ID: AKL 20403915113

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

OXYWISE S.R.O

Country of Origin

Slovakia

Authorized Representative

PT. OXY INDOMED

AR Address

Jl. Ir. H. Juanda Ruko 7 Rt 001/014 Kelurahan Kemiri muka, Kecamatan Beji Kota Depok

Registration Date

Dec 14, 2022

Expiry Date

Dec 31, 2027

Product Type

Therapeutic Anesthesia Equipment

Oxygen Generator System

Non Radiation Electromedics

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