SABER ™ Percutaneous Transluminal Angioplasty (PTA) Dilation Catheter - Indonesia BPOM Medical Device Registration
SABER ™ Percutaneous Transluminal Angioplasty (PTA) Dilation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501321118. The device is manufactured by NITINOL DEVICES & COMPONENTS from Costa Rica, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is WEGO MEDIKA INDONESIA.
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SABER ™ Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter
Risk Classification
Product Class
Kelas : 2
Manufacturer
NITINOL DEVICES & COMPONENTSCountry of Origin
Costa Rica
Authorized Representative
WEGO MEDIKA INDONESIAAR Address
Jl. Tanah Abang II No.67 Kel. Petojo Selatan, Kec. Gambir, Jakarta Pusat
Registration Date
Oct 31, 2023
Expiry Date
May 01, 2028
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile

