30 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LANX FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Procure Blood Pressure Monitor, Digital, Auto Inflate w/ Batteries
FDA UDI
PROACTIVE MEDICAL PRODUCTS, LLC·05060488570926·Procure Blood Pressure Monitor, Digital, Auto I...
neria™
FDA UDI
Unomedical A/S·05705244000292·Single use infusion set for subcutaneous infusi...
neria™
FDA UDI
Unomedical A/S·05705244021938·Single use infusion set for subcutaneous infusi...
thalaset™
FDA UDI
Unomedical A/S·05705244001336·Single use infusion set for subcutaneous infusi...
thalaset™
FDA UDI
Unomedical A/S·05705244005419·Single use infusion set for subcutaneous infusi...
BAYER RAPIDPOINT 400 SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SYMPHONY GRAFT DELIVERY SYSTEM (GDS)
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
DURAGEN-UNKNOWN PRODUCT ID
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORPORATION·Product code GXQ·January 17, 2012
DURAGEN-UNK PRODUCT ID
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORP.·Product code GXQ·January 17, 2012
DURAGEN-UNKNOWN PRODUCT ID
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORPORATION·Product code GXQ·January 17, 2012
DURAGEN-UNKNOWN PRODUCT ID
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORPORATION·Product code GXQ·January 17, 2012
ARSTASIS ACCESS SYSTEM
FDA Adverse Event
Other
·ARSTASIS INC.·Product code DYB·November 15, 2010
ARSTASIS ACCESS SYSTEM
FDA Adverse Event
Malfunction
·ARSTASIS, INC.·Product code DYB·November 19, 2010
ARSTASIS ACCESS SYSTEM
FDA Adverse Event
Other
·ARSTASIS, INC.·Product code DYB·November 22, 2010
ARSTASIS ACCESS SYSTEM
FDA Adverse Event
Injury
·ARSTASIS, INC.·Product code DYB·November 1, 2010
PURITAN BENNETT 980 SERIES VENTILATOR
FDA Adverse Event
Malfunction
·MEDTRONIC/COVIDIEN·Product code CBK·September 17, 2025
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 23, 2011
DETACH A TIP FENESTRATED GRASPER
FDA Adverse Event
Injury
·CONMED CORPORATION·Product code GEI·May 9, 2013
IN-SITU PLATE CUTTER, UPPERFACE/MIDFACE
FDA Adverse Event
Malfunction
·STRYKER LEIBINGER-FREIBURG·Product code LXH·September 19, 2014