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 30505420148. 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 20th Floor Jl. Jend. Sudirman Kav 45-46
Registration Date
Nov 15, 2024
Expiry Date
Sep 09, 2028
Product Type
Therapeutic Cardiology Equipment
Peripheral Stent (cardiology use)
Non Electromedic Sterile
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