8 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LAPAROSCOPIC INSTRUMENTS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471123083·K-WIRE - DOUBLE TROCAR 1.1mm DIA x 100mm
GUIDE WIRE EXTENSION
FDA 510(k)
FDA Class 2
·Cardiovascular
A.P.GRAPH III(TM) CARDIOVASCULAR ANALYZER
FDA 510(k)
FDA Class 2
·Cardiovascular
ENDOLOOP LIGATURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GEA·December 27, 2018
GRANUFLO
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 18, 2014
CONE BODY TRIAL TRAY #2 RESTORATION MODULAR
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·November 23, 2010
PELVISOFT ACELLULAR COLLAGEN BIOMESH
FDA Adverse Event
Injury
·TISSUE SCIENCE LABORATORIES·Product code FTM·January 17, 2013