IOXYGEN Medical Pressure Regulator - Indonesia BPOM Medical Device Registration
IOXYGEN Medical Pressure Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402220006. The device is manufactured by MORRIS PRECISION TECHNOLOGY CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDISTRON ENERGY.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MORRIS PRECISION TECHNOLOGY CO., LTD.Country of Origin
Taiwan (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
Oct 31, 2024
Expiry Date
Nov 14, 2027
Product Type
Monitoring Anesthesia Equipment
Pressure regulator.
Non Electromedic Non Sterile
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