24 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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VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR FOR VAPORIZED (VH2O2) STERILIZATION PROCESSES
FDA 510(k)
FDA Class 2
·General Hospital
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526827868·***DISC*LEVAMED ANKLE SUPPORT BLACK IV
LEONE SPA
FDA UDI
LEONE SPA·08033707065890·EXTRAORAL ELASTICS 3/8" 14 oz
Symmetry Surgical
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482038703·Symmetry® Probe, Double-Ended, Stainless Steel,...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450212592·
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·December 17, 2014
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962108734·00842962108734 HNM-1-09-0514 PROBE, 5 1/2", DOU...
PULPDENT GLAZE II
FDA 510(k)
FDA Class 2
·Dental
RUMBAR DRAINAGE SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
VKMO 78000 3 QUADROX-I HMO 70000+VHK7000
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 25, 2015
VKMO 78000 #QUADROX-I HMO 70000+VHK7000
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 25, 2015
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·February 20, 2014
BE-VKMO 70000 #QUADR-I HMO70000+VHK7100
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015
BE-VKMO 70000 #QUAD-I HMO70000+VHK7100
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015
BE-VKMO 70000 #QUADR-I HMO70000+VHK7100
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015
HLM TUBING SET W/SOFTLINE COATING
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DWF·April 6, 2016
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 9, 2018
BE-VEMO 7000 #QUADR-I HMO70000+VHK7100
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015
SENSOR?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code EZB·May 2, 2013
BATTERY CAP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·September 15, 2014