IOXYGEN Medical Double Flowmeter - Indonesia BPOM Medical Device Registration
IOXYGEN Medical Double Flowmeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402220007. 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 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
MEDISTRON ENERGYAR Address
Ruko Cinere Terrace Commercial Blok JC No. 5, Jl. Telaga Warna, Kecamatan Cinere, Kelurahan Pangkalan Jati
Registration Date
Oct 28, 2024
Expiry Date
Nov 14, 2027
Product Type
Monitoring Anesthesia Equipment
Compensated thorpe tube flowmeter.
Non Electromedic Non Sterile
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