8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SOFT TISSUE BIOPSY NEEDLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DYNASTY ACETABULAR SYSTEM
FDA 510(k)
FDA Class 3
·Orthopedic
MONITOR, RESPIRATORY, TWO-GAS, RDC
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
OXF ANAT BRG LT MD SIZE 4 PMA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JWH·May 1, 2018
OXF TWIN-PEG CMNTD FEM MD PMA
FDA Adverse Event
Injury
·.·Product code JDI·May 1, 2018
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·June 12, 2014
ARTICULEZE M 28MM 5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·December 12, 2012
RENEW DUAL RECEIVER, 16-CHANNEL
FDA Adverse Event
Malfunction
·ADVANCED NEUROMODULATION SYSTEMS·Product code GZB·September 29, 2010