9 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONS
FDA 510(k)
FDA Class 2
·Anesthesiology
G4 NiTi Lingual Wire .010 Small Lower
FDA UDI
SPECIALTY APPLIANCES, LLC·D8199512460·
GDC POWER SUPPLY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - FREMONT·Product code HCG·July 20, 2010
Aneroid Sphygmomanometer
FDA 510(k)
FDA Class 2
·Cardiovascular
CONSTRUX MINI PEEK VBR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MALLINCKRODT
FDA Adverse Event
Malfunction
·COVIDIEN·Product code BTR·August 17, 2016
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 8, 2013
TRAUMA TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·December 14, 2010
MINICAP TRANSFER SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 22, 2014