34 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GDS-DCS
FDA 510(k)
FDA Class 2
·Cardiovascular
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450450567·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450407356·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450434369·
EXCEL FRACTURE CEMENTED HIP STEM
FDA 510(k)
FDA Class 2
·Orthopedic
FAST-CATH 18F HEMOSTASIS INTRODUCER, MODEL 406XXX
FDA 510(k)
FDA Class 2
·Cardiovascular
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·January 9, 2014
ROD, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019
3.0MM TI CERVICAL SPINE LOCKING SCREW 16MM
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code OVE·May 3, 2013
GRANUFLO
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·August 28, 2014
3.3MM DRILL 25MM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·May 5, 2011
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·September 25, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·September 26, 2018
UPJ OCCLUSION BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZN·April 7, 2017
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·July 8, 2019
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·November 14, 2017
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·November 19, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·July 19, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·August 1, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·August 22, 2018