8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CARTO3 EP NAVIGATION SYSTEM, VERSION 3.2
FDA 510(k)
FDA Class 2
·Cardiovascular
ELMED
FDA UDI
ELMED INCORPORATED·00842180187290·Coller artery forceps. Crile-type forceps. Deli...
MISONIX SONICONE(R) ULTRASONIC WOUND CARE SYSTEM AND ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PARAGON HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MYSPINE STANDARD DRILL GUIDE T07
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code MNI·May 10, 2019
TAPERED U-JOINT DRIVER FOR SYNFIX MINI-OPEN
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code MAX·May 29, 2013
RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEI·June 17, 2011
CLIN CHEM BILIRUBIN CALIBRATOR
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING, INC.·Product code JIX·August 19, 2008