34 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BEST BREAST BRACHYTHERAPY APPLICATOR
FDA 510(k)
FDA Class 2
·Radiology
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809870626·FOR MEN 20-30 MM HG THIGH MICRO DOT BAND CLOSED...
ANTERIOR STABILIZED TIBIAL BEARINGS
FDA 510(k)
FDA Class 2
·Orthopedic
MEDPOR PTERIONAL SURGICAL IMPLANT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EXCELSIOR MICROCATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code DQY·April 13, 2010
EXCELSIOR SL-10 MICROCATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC, NEUROVASCULAR DIV.·Product code DQY·July 10, 2009
EXCELSIOR SL-10 PRE-SHAPED 45 CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQO·December 12, 2007
RED DCI-DC3 SENSOR
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·September 15, 2015
EXCELSIOR SL-10 PRE-SHAPED 45 DEGREES MICROCATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIV·Product code DQO·April 25, 2007
RD SET GE - 12
FDA Adverse Event
Malfunction
·Product code DQA·August 13, 2021
EXCELSIOR SL-10 PRE-SHAPED 45 DEGREES MICROCATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQO·November 14, 2007
EXCELSIOR SL-10 MICROCATHETER
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code DQO·May 1, 2007
EXCELSIOR SL-10 PRE-SHAPED CATHETER
FDA Adverse Event
Malfunction
·NEUROVASCULAR, A DIV. OF BOSTON SCIENTIFIC CORP·Product code DQO·September 14, 2006
EXCELSIOR SL-10 MICROCATHETER
FDA Adverse Event
Malfunction
·NEUROVASCULAR, A DIV OF BOSTON SCIENTIFIC CORP·Product code DQO·January 3, 2007
EXCELSIOR SL-10 MICROCATHETER
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIV·Product code DQO·September 15, 2006
EXCELSIOR SL-10 PRE-SHAPED 45 DEGREES MICROCATHER
FDA Adverse Event
Malfunction
·NEUROVASCULAR, DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code DQO·January 3, 2007
EXCELSIOR SL-10 PRE-SHAPED J MICROCATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code DQO·August 17, 2007
HOLLOW FIBER OXY WITH 3000 ML
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTZ·April 4, 2013
COLLEAGUE CX TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·April 6, 2011
VITALITY 2 VR
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008