36 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NONSTERILE POWDERED PURPLE LATEX EXAMINATION GLOVES, WITH & WITHOUT GRAPE SCENT WITH PROTEIN LABELING (200 MICROGRAMS OR
FDA 510(k)
FDA Class 1
·General Hospital
Elite Expandable Interbody Fusion System
FDA UDI
SPINEOLOGY INC.·M7403010095·9mm Paddle Distractor
Integrity-SI Fusion System
FDA UDI
Lincotek Medical LLC·B57112521010095D0·10 x 95 mm Anodized SI Implant
6.5 Cancellous Bone Shaft Screw, hex, St.Steel, L 95/16 mm
FDA UDI
mahe medical gmbh·EMAH00100100950·6.5 Cancellous Bone Shaft Screw, hex,
St.Ste...
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033088128·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033088159·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033260425·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033260173·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033260180·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033088234·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033354360·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033088142·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033088135·
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659173439·6.5 Cancellous Bone Shaft Screw, hex, _x000D_...
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033088166·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033088173·
OXYGEN SENSORS, MODELS CIR, C2R, R13, R15, RI7MED, R22MED, R23, R24MED, R29MED, T1, T2,T4, T7 & UFO130
FDA 510(k)
FDA Class 2
·Anesthesiology
OLYMPUS SONOSURG TROCAR XT3900 SYSTEM
FDA 510(k)
FDA Unclassified
·Unknown
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·March 8, 2011