GENTEC OXYBLEND Air/O2 Blender - Indonesia BPOM Medical Device Registration
GENTEC OXYBLEND Air/O2 Blender is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420017. The device is manufactured by GENTEC (SHANGHAI) CORPORATION from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDISTRON ENERGY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GENTEC (SHANGHAI) CORPORATIONCountry of Origin
China
Authorized Representative
PT. MEDISTRON ENERGYAR Address
Ruko Cinere Terrace Commercial Blok JC No. 5, Jl. Telaga Warna, Kecamatan Cinere, Kelurahan Pangkalan Jati
Registration Date
Jan 10, 2024
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Anesthesia Equipment
Breathing gas mixer.
Non Electromedic Non Sterile
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