8 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REINFORCED SILICONE TRACHEAL TUBE
FDA 510(k)
FDA Class 2
·Anesthesiology
MONDEAL
FDA UDI
MONDEAL Medical Systems GmbH·04050435062339·MCD Screw 3.0 x 52 mm cannulated M2
partia...
iNSitu Hip System
FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127025891·Acetabular Reamer, Full Hemisphere, Crossbar, 52mm
PACEMAKER, ELECTRODE
FDA 510(k)
FDA Class 3
·Cardiovascular
Tornier Humeral Nail and Tornier Long Humeral Nail
FDA 510(k)
FDA Class 2
·Orthopedic
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·May 12, 2014
MX-PRO R-3 AMBULANCE COT
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·October 10, 2012
ENDOPATH XCEL BLUNT TIP TROCAR
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GCJ·January 10, 2008