CAPIOX RX Hollow Fiber Oxygenator with Hardshell Reservoir - Indonesia BPOM Medical Device Registration
CAPIOX RX Hollow Fiber Oxygenator with Hardshell Reservoir is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504120160. The device is manufactured by TERUMO CARDIOVASCULAR SYSTEMS CORPORATION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIONCountry of Origin
United States
Authorized Representative
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
May 20, 2023
Expiry Date
Apr 10, 2028
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass oxygenator.
Non Electromedic Sterile
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