Vivo ISAR - Indonesia BPOM Medical Device Registration
Vivo ISAR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503220083. The device is manufactured by TRANSLUMINA THERAPEUTICS LLP from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is ARQON MEDICAL SOLUTIONS.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
TRANSLUMINA THERAPEUTICS LLPCountry of Origin
India
Authorized Representative
ARQON MEDICAL SOLUTIONSAR Address
Rukan Niaga Gunung Sahari Blok B2 Jl Gunung Sahari Raya No 7
Registration Date
Aug 18, 2022
Expiry Date
Mar 31, 2027
Product Type
Prosthetic Cardiology Equipment
Drug eluting stent
Non Electromedic Sterile
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