Vienna Valve: Transcatheter Aortic Valve System - Indonesia BPOM Medical Device Registration
Vienna Valve: Transcatheter Aortic Valve System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503320321. The device is manufactured by RELISYS MEDICAL DEVICES LTD from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is AGRAPANA MULIA MEDIKA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
RELISYS MEDICAL DEVICES LTDCountry of Origin
India
Authorized Representative
AGRAPANA MULIA MEDIKAAR Address
ITC Cempaka Mas Mega Grosir Lantai 8 No 8A Jl. Letjend Suprapto Kav.1
Registration Date
Oct 25, 2023
Expiry Date
Jul 10, 2028
Product Type
Prosthetic Cardiology Equipment
Prosthesis Percutaneously Delivered Aortic Valve
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