ULTRAVERSE ™ 014 PTA Balloon Dilation Catheter - Indonesia BPOM Medical Device Registration
ULTRAVERSE ™ 014 PTA Balloon Dilation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420434. The device is manufactured by CLEARSTREAM TECHNOLOGIES LTD. from Ireland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BECTON DICKINSON INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CLEARSTREAM TECHNOLOGIES LTD.Country of Origin
Ireland
Authorized Representative
BECTON DICKINSON INDONESIAAR Address
Sampoerna Strategic Square South Tower 20th Floor Jl. Jend. Sudirman Kav 45-46
Registration Date
Aug 12, 2024
Expiry Date
May 16, 2029
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile
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