AIRSEP Oxygen Concentrator - Indonesia BPOM Medical Device Registration
AIRSEP Oxygen Concentrator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403122464. The device is manufactured by CAIRO INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ARIMIA JAYA MANDIRI.
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
CAIRO INC.Country of Origin
United States
Authorized Representative
PT. ARIMIA JAYA MANDIRIAR Address
Gedung Konica lantai 3A Jl. Gunung Sahari Raya nomor 78
Registration Date
Jul 29, 2024
Expiry Date
Mar 18, 2028
Product Type
Therapeutic Anesthesia Equipment
Portable oxygen generator.
Non Radiation Electromedics
AIRSEP Oxygen Concentrator
CAIRE MEDICAL TECHNOLOGY (CHENGDU) CO., LTD.
CAIRE Oxygen Concentrator
CAIRE MEDICAL TECHNOLOGY (CHENGDU) CO., LTD.
VIDAMED Neonatal Incubator
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD
VIDAMED Infant Phototherapy
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD
VIDAMED Defibrillator Monitor
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD
VIDAMED Defibrillator Monitor
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD
VIDAMED Neonatal Incubator
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD

