Biedermann Motech GmbH & Co. KG
4 devices · 5 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.
- NA 109-015-1436Intervertebral fusion device with bone graft, lumbar2 reports
- NA 109-015-1032Intervertebral fusion device with bone graft, lumbar1 report
- NA 209-010-0502ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 208-040-0409ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report