31 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MICROLIGHT 830 LASER SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
Blades key
FDA UDI
Spiggle & Theis Medizintechnik GmbH·04250676746665·1 piece
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756814324·RIGID COLLAR
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033111512·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033111574·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033111482·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033111536·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033111475·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033111499·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033111550·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033111505·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033111581·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197026314·Standard Operating Scissors Fig. 1
straig...
SERAGARD VASCULAR ACCESS PATCH
FDA 510(k)
FDA Class 2
·General Hospital
HARDYDISK TICARILLIN 75MCG
FDA 510(k)
FDA Class 2
·Microbiology
RESTORE
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·December 17, 2012
RESTORE
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 24, 2014
RESTORE
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 4, 2013
PENUMBRA SYSTEM REPERFUSION CATHETER 032
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·February 4, 2011
2520274-2013-01510
FDA Adverse Event
Injury
·SYNTHES USA·Product code MQP·March 19, 2013