62 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Dental Computed Tomography X-Ray System, Green X
FDA 510(k)
FDA Class 2
·Radiology
Dornier MedTech
FDA UDI
Dornier MedTech GmbH·04049958000218·Medilas D LiteBeam+ Diode Laser, D-Plug
CODMAN
FDA UDI
Cerenovus, Inc.·10886704001355·CODMAN SLIM-LINE Aneurysm Clip Right Angle Blad...
ABSORBENT PAPER POINTS
FDA UDI
DiaDent Group International·08806383512619·"An absorbent paper points is an endodontic pap...
SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE
FDA 510(k)
FDA Class 2
·Microbiology
TRIFIX SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
OTHER
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 27, 2011
TENSION FREE VAGINAL TAPE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·January 8, 2019
ARCHITECT SHBG
FDA Adverse Event
Malfunction
·ABBOTT GERMANY·Product code CDZ·May 8, 2017
TENSION FREE VAGINAL TAPE - OBTURATOR UNKNOWN PROD
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·October 9, 2018
TENSION FREE VAGINAL TAPE - OBTURATOR UNKNOWN PROD
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·October 5, 2018
TENSION FREE VAGINAL TAPE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·October 15, 2018
TENSION FREE VAGINAL TAPE - OBTURATOR UNKNOWN PROD
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·October 5, 2018
TENSION FREE VAGINAL TAPE - OBTURATOR UNKNOWN PROD
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·January 2, 2019
ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAT·February 21, 2019
TENSION FREE VAGINAL TAPE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·January 2, 2019
COREVALVE 31MM AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·October 27, 2014
MICRBR GEMSTR 1.2 FLTR PP Y-SITE 96IN
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·June 26, 2013
REVO MRI SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC S.A.·Product code LWP·August 11, 2011
RF3000 RADIOFREQUENCY GENERATOR
FDA Adverse Event
Injury
·STELLARTECH RESEARCH CORPORATION·Product code GEI·October 20, 2017