VitaFlow Liberty ™ Transcatheter Aortic Valve System - Indonesia BPOM Medical Device Registration
VitaFlow Liberty ™ Transcatheter Aortic Valve System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503320327. The device is manufactured by SHANGHAI MICROPORT CARDIOFLOW MEDTECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. UBC MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
SHANGHAI MICROPORT CARDIOFLOW MEDTECH CO., LTDCountry of Origin
China
Authorized Representative
PT. UBC MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930
Registration Date
Oct 29, 2023
Expiry Date
Jul 26, 2028
Product Type
Prosthetic Cardiology Equipment
Prosthesis Percutaneously Delivered Aortic Valve
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