9 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MASTERSCREEN BODY
FDA 510(k)
FDA Class 2
·Anesthesiology
Reef TH
FDA UDI
Seaspine Orthopedics Corporation·10889981202842·Interbody, 9mm x 36mm x 10mm, 8 deg
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981194857·Interbody, 9mm x 36mm x 10mm, 8 deg
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0361080·Compressor, Fixed Tip
RMHS POROUS DISTAL SLEEVE
FDA 510(k)
FDA Class 2
·Orthopedic
VINGMED SOUND COLOR FLOW MAPPING SYSTEM, CFM-800
FDA 510(k)
FDA Class 2
·Radiology
STAR S4-IR-ETL EXCIMER LASER
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code LZS·January 30, 2013
MICRO-DRIVER RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MAF·December 13, 2010
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 15, 2014