32 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Bioflux Software II
FDA 510(k)
FDA Class 2
·Cardiovascular
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772344123·PROTECT.PRO ACTION BACK SUPPORT BLACK L
LoFric® Hydro-Kit™
FDA UDI
Wellspect AB·07392532138614·Single Use Urinary Catheter LoFric Hydro-Kit Ne...
Pantheon System
FDA UDI
ADLER ORTHO SPA·08050880238231·Pantheon Bridging Collar Ø 26 mm for Stem Ø 14 mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694036474·Goniometer
Life Instruments
FDA UDI
Life Instrument Corporation·M9307201040S0·Pedicle Curette # 4/0 with Stop
Preference
FDA UDI
CTL Medical Corporation·00841732152007·7.2mm Polyaxial Screw Reduction 40mm Green
Viceroy
FDA UDI
DIOMEDICAL CO.,LTD.·08800039826143·Rod 6.0 x 40mm
Silhouette Instalift
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Universal Base Conical Connection (CC)
FDA 510(k)
FDA Class 2
·Dental
ACCESS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - AIBONITO·Product code FRN·October 27, 2014
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·July 1, 2011
CURVED PLATE, 5 HOLES, LEFT
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS-FREIBURG·Product code HRS·July 2, 2013
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·March 17, 2015
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·March 17, 2015
ENDEAVOR RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·July 28, 2010
ENDEAVOR RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·July 28, 2010
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·March 17, 2015
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·March 17, 2015
MICRUS MICROCOIL SYSTEM
FDA Adverse Event
Injury
·MICRUS ENDOVASCULAR CORPORATION·Product code HCG·February 28, 2012