37 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
spineEOS rod Template
FDA UDI
ONEFIT MEDICAL·03700757200803·spineEOS rod template is intended to be designe...
spineEOS rod Template
FDA UDI
ONEFIT MEDICAL·03700757200766·spineEOS rod template is intended to be designe...
spineEOS
FDA UDI
ONEFIT MEDICAL·03700757200858·spineEOS 1.x allows surgeons to perform preoper...
spineEOS rod Template
FDA UDI
ONEFIT MEDICAL·03700757200797·spineEOS rod template is intended to be designe...
hipEOS
FDA UDI
ONEFIT MEDICAL·03700757200834·hipEOS allows surgeons to perform pre-operative...
spineEOS rod Template
FDA UDI
ONEFIT MEDICAL·03700757200773·spineEOS rod template is intended to be designe...
spineEOS rod Template
FDA UDI
ONEFIT MEDICAL·03700757200780·spineEOS rod template is intended to be designe...
kneeEOS
FDA UDI
ONEFIT MEDICAL·03700757200506·kneeEOS allows surgeons to perform preoperative...
spineEOS rod Template
FDA UDI
ONEFIT MEDICAL·03700757200643·spineEOS rod template is intended to be designe...
spineEOS rod Template
FDA UDI
ONEFIT MEDICAL·03700757200759·spineEOS rod template is intended to be designe...
spineEOS rod Template
FDA UDI
ONEFIT MEDICAL·03700757200650·spineEOS rod template is intended to be designe...
hipEOS
FDA UDI
ONEFIT MEDICAL·03700757200520·hipEOS allows surgeons to perform pre-operative...
hipEOS
FDA UDI
ONEFIT MEDICAL·03700757200827·hipEOS allows surgeons to perform pre-operative...
spineEOS
FDA UDI
ONEFIT MEDICAL·03700757200544·spineEOS allows surgeons to perform preoperativ...
NITE GUARD
FDA Adverse Event
Malfunction
·RANIR, LLC·Product code OBR·May 1, 2014
NITE GUARD
FDA Adverse Event
Malfunction
·RANIR, LC·Product code OBR·May 1, 2014
NITE GUARD
FDA Adverse Event
Malfunction
·RANIR, LLC.·Product code OBR·May 1, 2014
6F ANGIO-SEAL VIP VASCULAR CLOSURE DEVICE, US
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code MGB·November 27, 2023
FOUNDATION HIP
FDA Adverse Event
Other
·ENCORE MEDICAL, L.P.·Product code LPH·April 5, 2012
6F ANGIO-SEAL VIP VASCULAR CLOSURE DEVICE, US
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code MGB·November 27, 2023