6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ULTRASONIC HAND INSTRUMENTS
FDA 510(k)
FDA Unclassified
·Unknown
CATHETER, CEBTRAL VENOUS, 2N1501
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
CAPILLARYS Hb A1c
FDA 510(k)
FDA Class 2
·Clinical Chemistry
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON INC·Product code OTN·February 21, 2013
DREAMTOME RX SPHINCTEROTOME
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code KNS·January 27, 2011
DEPUY ASR XL FEM IMP SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·July 31, 2014