30 results
·
26ms
·
Sources: EU EUDAMED, US FDA
AURORA
FDA 510(k)
FDA Class 2
·Radiology
GRADIA®
FDA UDI
Gc America Inc.·14548161296564·GRADIA® CORE Kit (1CORE Cartridge 10 mL (20 g),...
GRADIA®
FDA UDI
Gc America Inc.·D0470036511·GRADIA® CORE Kit (1CORE Cartridge 10 mL (20 g),...
LINK Instruments - Drills, reamers and saw blades
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575157662·Bone trephine - Endo Model Knee System
EX-CELL 301, CATALOG NO. 200-3651
FDA 510(k)
FDA Class 1
·Hematology
BIO-RAD %CDT TIA
FDA 510(k)
FDA Class 1
·Clinical Chemistry
DETACH 18 AND DETACH 11, NEUROLOGICAL EMBOLIZATION COIL SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
HEPARIN LOCK FLUSH
FDA Adverse Event
Malfunction
·APP·Product code NZW·June 27, 2012
5.0MM FLEXIBLE SHAFT
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HTO·February 28, 2013
UNKNOWN ZIMMER KNEE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·February 23, 2011
ENDOSCOPIC MULTIFEED STAPLER - 360 ROTATION 20 TITANIUM STAPLES
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GCJ·February 14, 2008
BD 10ML SYRINGE LUER-LOK TIP
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 10, 2019
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 10, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 10, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 8, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 8, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 8, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 8, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 8, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 8, 2024