7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ProtekDuo Veno-Venous Cannula Sets
FDA 510(k)
FDA Class 2
·Cardiovascular
RIGIDLOOP
FDA UDI
S.B.M·03760304680175·The RIGIDLOOP device consists of an adjustable ...
AIR-FLOW HANDY 3.0 PERIO
FDA 510(k)
FDA Class 1
·Dental
AUTOSET SPIRIT SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
PUREPOINT
FDA Adverse Event
Malfunction
·ALCON-IRVINE TECHNOLOGY CTR·Product code HQF·October 28, 2014
TRIATHLON CR X3 TIBIAL INSERT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·August 25, 2011
ACCU-CHEK ® MULTICLIX
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·July 18, 2013