6 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DATUM
FDA 510(k)
FDA Class 2
·Anesthesiology
QRS-CARD CARDIOLOGY SUITE
FDA 510(k)
FDA Class 2
·Cardiovascular
Model BT-220L and BT-220C
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
5MM X 32CM STRYKEPROBE SPATULA TIP
FDA Adverse Event
Injury
·STRYKER ENDOSCOPY-SAN JOSE·Product code GEI·February 4, 2013
PUMP/GRAVITY CONTINUE INTERLINK
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MALTA·Product code FPA·December 30, 2010
MODEL NOT SPECIFIED
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code FPA·July 17, 2014