32 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BANICIDE LIQUID CHEMICAL STERILANT/HIGH-LEVEL DISINFECTANT
FDA 510(k)
FDA Class 2
·General Hospital
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130719·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130917·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130894·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130733·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130856·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130832·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130818·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130771·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130696·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130795·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130870·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304130757·
PNS MAGNETIC STIMULATOR SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
BABY DOPPLEX 3000 MK 2 (BD3000)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code DQY·December 8, 2006
ST. JOSEPH HSP BALTIMORE MD1
FDA Adverse Event
Other
·SORIN GROUP USA, INC.·Product code DWF·October 1, 2010
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCO·Product code CBK·March 1, 2013
ENDOPATH STEALTH CIR STAPLER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code KOG·March 10, 2011
LENOX VR-T
FDA Adverse Event
Malfunction
·BIOTRONIK GMBH AND CO.·Product code LWS·March 10, 2008