Integrum AB
16 devices · 144 adverse event reports · 0 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- OPRA Implant System 1288Transfemoral Percutaneous Prosthetic109 reports
- OPRA Implant System 1820Transfemoral Percutaneous Prosthetic8 reports
- OPRA Implant System 1800Transfemoral Percutaneous Prosthetic4 reports
- OPRA Implant System 1804Transfemoral Percutaneous Prosthetic4 reports
- OPRA Implant System 1808Transfemoral Percutaneous Prosthetic3 reports
- OPRA Implant System 1803Transfemoral Percutaneous Prosthetic2 reports
- OPRA Implant System 1810Transfemoral Percutaneous Prosthetic2 reports
- OPRA Implant System 1811Transfemoral Percutaneous Prosthetic2 reports
- OPRA Implant System IBC0010Transfemoral Percutaneous Prosthetic2 reports
- OPRA Implant System IBC0012Transfemoral Percutaneous Prosthetic2 reports
- OPRA Implant System 1342Transfemoral Percutaneous Prosthetic1 report
- OPRA Implant System 1348Transfemoral Percutaneous Prosthetic1 report
- OPRA Implant System 1353Transfemoral Percutaneous Prosthetic1 report
- OPRA Implant System 1805Transfemoral Percutaneous Prosthetic1 report
- OPRA Implant System 1807Transfemoral Percutaneous Prosthetic1 report
- OPRA Implant System 1959Transfemoral Percutaneous Prosthetic1 report