41 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DeRoyal Temperature Monitoring Probe
FDA 510(k)
FDA Class 2
·General Hospital
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777631·LUMBAMED BASIC DORSAL STAYS M SILVER I
Ceramco® iC
FDA UDI
Dentsply International Inc.·D00142006310·CC-311
Olympus
FDA UDI
Gyrus ACMI, LLC·00821925047266·ES-IP iOR BWK Hamburg OP (with rack)
OsteoMed
FDA UDI
OSTEOMED LLC·00845694017794·MFx 2.0/2.4mm Angulated Locking Fracture Organi...
Orthoquest
FDA UDI
Young Innovations, Inc.·00843471159071·T Ultra T° D-Form D014X025
Apelo® / Apelo® MIS
FDA UDI
ATLAS SPINE, INC.·M68120063100000·Straight Sounding Probe
AFFIITY CP CENTRIFUGAL BLOOD PUMP
FDA 510(k)
FDA Class 2
·Cardiovascular
IPLAN
FDA 510(k)
FDA Class 2
·Neurology
UNKNOWN
FDA Adverse Event
MEDTRONIC NEUROMODULATION·Product code LKK·October 11, 2007
VITOSS BONE GRAFT SUBSTITUTE
FDA Adverse Event
Injury
·Product code MQV·May 22, 2008
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008
SPRINT QUATTRO SECURE S
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 1, 2013
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 7, 2010
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 7, 2010
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 7, 2010
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 7, 2010
PYRAMESH IMPLANT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MQP·September 7, 2010
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 7, 2010