32 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DIDECO D901 LILLIPUT HOLLOW FIBER OXYGENATOR WITH OR WITHOUT SOFT VENOUS RESERVOIR BAG, WITH BIOCOMPATABLE TREATMENT SUR
FDA 510(k)
FDA Class 2
·Cardiovascular
DIDECO D901 LILLIPUT HOLLOW FIBER OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·September 15, 2022
DIDECO D901 LILLIPUT HOLLOW FIBER OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·September 14, 2022
Vivid NuFill Unit Dose Assorted
FDA UDI
PEARSON DENTAL SUPPLIES, INC.·D724D0104780·50 x .25g
AJL Vacuum Centering Guide
FDA UDI
AJL OPHTHALMIC SA·08435194334969·
Intacs Vacuum Centering Guide
FDA UDI
ADDITION TECHNOLOGY, INC.·00850048576056·The Vacuum Centering Guide (VCG) is composed of...
LEICA BIOSYSTEMS NUSSLOCH GMBH
FDA registration
LEICA BIOSYSTEMS NUSSLOCH GMBH·9 products·🇩🇪 Germany
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164327·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164341·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164310·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164303·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164334·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033164365·
IMPLANT: HA, INTEGRAL
FDA Adverse Event
Other
·CALCITEK·Product code DZE·February 7, 1997
THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/ RADIOTHERAPY V2.1
FDA 510(k)
FDA Class 2
·Radiology
AURECAST SUPER INLAY
FDA 510(k)
FDA Class 2
·Dental
8010478-2018-00005
FDA Adverse Event
Injury
·December 13, 2018
LEICA CM1520
FDA Adverse Event
Injury
·LEICA BIOSYSTEMS NUSSLOCH GMBH·Product code IDP·December 2, 2016
LEICA ASP300S
FDA Adverse Event
Injury
·LEICA BIOSYSTEMS NUSSLOCH GMBH·Product code IEO·October 7, 2013
LEICA ASP300S
FDA Adverse Event
Injury
·LEICA BIOSYSTEMS NUSSLOCH GMBH·Product code IEO·February 16, 2018