89 results
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31ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HARMONIC FOCUS SHEARS + ADAPTIVE TISSUE TECHNOLOGY
FDA 510(k)
FDA Unclassified
·Unknown
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1671333140·
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613025113·Reynolds (Jamison) Scissors, Super Cut, Curved,...
PROTEGE GPS SELF-EXPANDING NITINOL STENT AND DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CLOTRAC HEPARINASE TEST CARTIDGE (HTC) COAGULATION CONTROL
FDA 510(k)
FDA Class 2
·Hematology
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523147199·PS Tibia Insert Trial Size B, 14mm - Left
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172702·PS Tibia Insert Trial with Posterior Pin Relief...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144785·L UHMWPE PS Tibial Insert Sz B 14mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523142880·L E-CIMA Vitamin E PS Tibial Insert Sz B 14mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523143740·L CIMA HXL PS Tibial Insert Sz B 14mm
PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·July 22, 2015
PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·June 18, 2015
PENUMBRA SYSTEM JETD REPERFUSION CATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·May 8, 2019
PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·July 17, 2015
PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·October 30, 2015
PENUMBRA SYSTEM 3MAX REPERFUSION CATHETER
FDA Adverse Event
Injury
·PENUMBRA, INC.·Product code NRY·June 14, 2015
PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·June 26, 2015
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·October 1, 2014
ACCU-CHEK ® ULTRAFLEX INFUSION SET
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·May 29, 2013
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 20, 2011