26 results
·
24ms
·
Sources: EU EUDAMED, US FDA
MODIFICATION TO PLEURX PLEURAL CATHETER AND DRAINAGE KITS
FDA 510(k)
FDA Class 2
·Cardiovascular
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040012505·Zirlux 16+ C4 95X22
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526780798·LEVAMED ACTIVE ANKLE SUP SLVR R I
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077229·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077243·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077236·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077205·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077274·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077250·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077267·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077212·
AVIATOR PERIPHERAL DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
NEEDLELESS TRANSFER DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 8, 2025
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·October 26, 2025
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 8, 2025
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 8, 2025
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 8, 2025
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 8, 2025
ENDOPATH ETS
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code KOG·November 7, 1997