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ReOxy Breathing Therapy Device - Indonesia BPOM Medical Device Registration

ReOxy Breathing Therapy Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403911987. The device is manufactured by BITMOS GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is REGENESIS 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.

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BPOM Registered
Risk Class Kelas Resiko : B
ReOxy Breathing Therapy Device
Analysis ID: AKL 20403911987

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BITMOS GMBH

Country of Origin

Germany

Authorized Representative

REGENESIS INDONESIA

AR Address

Jalan Sultan Iskandar Muda No. 7 A dan B, Kebayoran lama Selatan, Kebayoran Lama, Jakarta Selatan

Registration Date

Oct 27, 2023

Expiry Date

Aug 10, 2028

Product Type

Therapeutic Anesthesia Equipment

Breathing gas mixer.

Non Radiation Electromedics

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