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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BITMOS GMBHCountry of Origin
Germany
Authorized Representative
REGENESIS INDONESIAAR 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

