9 results
·
34ms
·
Sources: EU EUDAMED, US FDA
SB ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
SafeClinitube D941P-NA-240-55
FDA UDI
Radiometer Medical ApS·05700699428899·SafeClinitube D941P-NA-240-55
CELT ACD VASCULAR CLOSURE DEVICE
FDA Adverse Event
Malfunction
·VASORUM LTD.·Product code MGB·July 30, 2024
ATTUNE FEM POR PS RT SZ 9
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code MBH·September 22, 2025
DYNAMOMETER - MODEL FCE AND MODEL MSC
FDA 510(k)
FDA Class 2
·Orthopedic
Celerity PICC Tip Confirmation System
FDA 510(k)
FDA Class 2
·General Hospital
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 5, 2013
INTEGRIS V5000
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code IZI·December 16, 2010
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 17, 2014