7 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
RELEASABLE FORCE MODULE
FDA 510(k)
FDA Class 2
·Dental
DeltaForm HD
FDA UDI
Merz Dental GmbH·D7091980151·DeltaForm HD lower posteriors, XL, D4 -MADE IN ...
ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076 AND 2039
FDA 510(k)
FDA Class 2
·Cardiovascular
MC3 Jugular Dual Lumen Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
EVITA
FDA Adverse Event
Malfunction
·DRAEGER MEDICAL GMBH·Product code CBK·February 19, 2013
8800
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE, LTD.·Product code JAA·January 24, 2011
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 5, 2014