23 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIPAP PLUS M-SERIES BI-LEVEL SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
ENCOREANYWHERE
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·February 17, 2016
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T0610340·6mm TLIF Implant 10mm Wide 34mm Length
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70610341·Mini Sprint-Brackets 5-5 McLaugh/Benn/Trev. .01...
MODEL APS ALTERNANS PROCESSING SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
SYNTHES (USA) MEDIUM EXTERNAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710610340090·Tri-Channel Met-Traverse, 34mm x 9mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710610340100·Tri-Channel Met-Traverse, 34mm x 10mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710610340080·Tri-Channel Met-Traverse, 34mm x 8mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710610340070·Tri-Channel Met-Traverse, 34mm x 7mm
RU NOVOSIBIRSK
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTZ·October 16, 2013
ST JOSEPHS PHOENIX, AZ 1
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code DWF·July 31, 2009
RU NOVOSIBRIRSK
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTZ·April 11, 2013
RU NOVOSIBIRSK
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DWF·October 16, 2013
CP87170 DE MUENCHEN
FDA Adverse Event
Death
·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011
E500 VENTILATOR SYSTEM
FDA Adverse Event
Injury
·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·July 11, 2016
TRIGEN TAN D LT LIME
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JDS·April 16, 2013
5803 ADVANCED CONTROL BASE
FDA Adverse Event
Other
·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code GDC·March 16, 2011
HEARTSTREAM XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 12, 2008
CP87641 GB SOUTHAMPTON
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DWE·March 22, 2010