18 results
·
21ms
·
Sources: EU EUDAMED, US FDA
COCHLEAR BAHA BP100
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
DUFNER Instrumente GmbH
FDA UDI
DUFNER - Instrumente GmbH Fabrik ärztlicher Instrumente Medizintechnik·04063763199691·MICTEC Flexible trocar set TITANIUM, Ø7 mm, 100...
TITANIUM MICTEC FLEXIBLE TROCAR SET
FDA UDI
SONTEC INSTRUMENTS, INC.·B09920907200·TITANIUM MICTEC FLEXIBLE TROCAR SET
TITANIUM MICTEC FLEXIBLE TROCAR SET
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896007819·TITANIUM MICTEC FLEXIBLE TROCAR SET
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·October 26, 2017
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·October 26, 2017
BD LUER-LOK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·March 12, 2019
SOMNUS DISPOSABLE TISSUE COAGULATING ELECTRODE AND SOMNUS REUSABLE CONNECTOR CABLE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TSRH SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·March 6, 2019
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·August 24, 2016
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 10, 2016
MEDISORB¿ MULTI-ABSORBER ORIGINAL, DISPOSABLE
FDA Adverse Event
Malfunction
·Product code CBL·June 23, 2021
BD LUER-LOK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 25, 2019
FUSION NAVIGATION SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·May 2, 2013
PULSE GEN MODEL 102
FDA Adverse Event
Death
·CYBERONICS, INC.·Product code LYJ·September 15, 2014
S3 SHOULDER PLATE 3 HOLE RIGHT
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS, INC.·Product code LXT·April 29, 2011
BD LUER-LOK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·April 12, 2019