VENOVO™ Venous Stent System - Indonesia BPOM Medical Device Registration
VENOVO™ Venous Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503320364. The device is manufactured by ANGIOMED GMBH & CO. MEDIZINTECHNIK KG from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. BECTON DICKINSON INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
ANGIOMED GMBH & CO. MEDIZINTECHNIK KGCountry of Origin
Germany
Authorized Representative
PT. BECTON DICKINSON INDONESIAAR Address
SAMPOERNA STRATEGIC SQUARE, SOUTH TOWER LT.20 JL. JEND SUDIRMAN KAV 45-46
Registration Date
Dec 28, 2023
Expiry Date
Sep 09, 2028
Product Type
Prosthetic Cardiology Equipment
Coronary stent
Non Electromedic Sterile
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