10 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ENLUXTRA HUMIFIBER WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197041379·TC Super-Cut Stevens Tenotomy Scissors
curved...
AUTO SUTURE POWERED MULTIFIRE ENDO GIA 60-4.8
FDA Adverse Event
Injury
·UNITED STATES SURGICAL CORP.·Product code GCJ·November 12, 1997
GLOBAL ECG MANAGEMENT SYSTEM (GEMS)
FDA 510(k)
FDA Class 2
·Cardiovascular
ORIGIN HIP STEM, FEMORAL HEAD, LOGICAL PX-SERIES ACETABULAR SHELL, LOCIGAL G-SERIES ACETABULAR SHELL, LOGICAL ACETABULAR
FDA 510(k)
FDA Class 2
·Orthopedic
INFLATOR KIT 18INFKIT BALLOON
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code LRC·August 15, 2014
BALLOON SEEKER
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code LRC·August 15, 2014
U BY KOTEX SLEEK
FDA Adverse Event
Malfunction
·AVENT S. DE R.L. DE C.V.·Product code HEB·May 21, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 18, 2014
ROTATING MULTIPLE CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 13, 2011