931 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
AETOS Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556812068·BASEPLATE PIN GUIDE ECCENTRIC
AETOS Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556812037·BASEPLATE PIN GUIDE CONCENTRIC
Titan Reverse Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556863848·ECCENTRIC WIRE GUIDE WITH LIP
AETOS Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556812051·BASEPLATE PIN GUIDE 15 DEG FW
AETOS Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556812044·BASEPLATE PIN GUIDE 10 DEG FW
Titan Reverse Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556863855·RSS GLENOID BASEPLATE WIRE GUIDE
Titan Reverse Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556863831·CONCENTRIC WIRE GUIDE WITH LIP
WAVEON CRX GWG
FDA Adverse Event
Injury
·SONOMA ORTHOPEDIC PRODUCTS INC.·Product code HSB·March 5, 2010
WAVEON CRX GWG
FDA Adverse Event
Injury
·SONOMA ORTHOPEDIC PRODUCTS INC.·Product code HSB·October 1, 2009
Titan™
FDA UDI
Ascension Orthopedics, Inc.·10381780245438·Titan™ Reverse Shoulder System
The glenoid wire...
Titan™
FDA UDI
Ascension Orthopedics, Inc.·10381780245414·Titan™ Reverse Shoulder System
The glenoid wire...
Titan™
FDA UDI
Ascension Orthopedics, Inc.·10381780245421·Titan™ Reverse Shoulder System
The glenoid wire...
NONE
FDA Adverse Event
Malfunction
·GEOMED MEDIZIN-TECHNIK GMBH & CO.·Product code GWG·October 10, 2011
MINOP INVENT BIPOLAR 40DG D2.7MM L310MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GWG·December 1, 2016
APOLLO WAND
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code GWG·July 16, 2015
APOLLO SYSTEM APOLLO WAND
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code GWG·June 23, 2014
NEURO BALLOON CATHETER
FDA Adverse Event
Malfunction
·INTEGRA NEUROSCIENCES IMPLANTS SA·Product code GWG·June 5, 2014
APOLLO PUMP
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code GWG·July 16, 2015
APOLLO SYSTEM GENERATOR
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code GWG·September 3, 2015
KARL STORZ
FDA Adverse Event
Malfunction
·KARL STORZ GMBH & CO. KG·Product code GWG·May 9, 2014