13 results
·
20ms
·
Sources: EU EUDAMED, US FDA
RAPIDEC STAPH
FDA 510(k)
FDA Class 1
·Microbiology
Zavation
FDA UDI
Zavation LLC·00197157004064·Curved Bone Probe, 3.25 TIP
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613327370690·FACIAL ID-RECON-4PLATES
Persona®
FDA UDI
Zimmer, Inc.·00889024560444·
Persona®
FDA UDI
Zimmer, Inc.·00889024557796·
Persona®
FDA UDI
Zimmer, Inc.·00889024560222·
FLOW MED 160
FDA 510(k)
FDA Class 2
·General Hospital
Advocate Non-Contact Infrared Thermometer
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
Zimmer, Inc.·00889024065314·
SCREWDRIVER SHAFT, COMPRESSION T2 TIBIA 3.5 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code HXX·July 27, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·December 31, 2012
PULSE GEN MODEL 102
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·October 29, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 31, 2014