12 results
·
27ms
·
Sources: EU EUDAMED, US FDA
LIEBERMAN POLACK DOUBLE CORNEAL FORCEPS
FDA 510(k)
FDA Class 1
·Ophthalmic
Darby Dental Supply, LLC
FDA UDI
DARBY DENTAL SUPPLY, LLC·00889813056288·WIRE NI-TEK UPPER .017X.025 PKG/10
NA
FDA UDI
KEY SURGICAL, INC.·00849771048176·K-Wire and Steinmann Pin Dispensers, .045-inch...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292244·DISP K-WIRE FOR .045" (1.1MM) 6.25"
K-Wire and Steinmann Pin Dispensers
FDA UDI
KEY SURGICAL, INC.·00849771011996·K-Wire and Steinmann Pin Dispensers, .045-inch...
STAPLIZER
FDA UDI
Conmed Corporation·10845854016299·STAPLIZER BONE STAPLE CARTRIDGE, 7 X 10 MM
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197073691·Center Blade for Henley Retractor
32x16 mm
3M Attest Rapid Readout Biological Indicator, 3M Attest Auto-reader
FDA 510(k)
FDA Class 2
·General Hospital
CHARNLEY CONGENITAL HIP FEMUR (85-3061)
FDA 510(k)
FDA Class 2
·Orthopedic
COAGUCHEK XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·November 13, 2007
XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·October 3, 2012
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·December 18, 2013