6 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STERRAD STERILIZATION POUCH
FDA 510(k)
FDA Class 2
·General Hospital
I-D GLIDE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Biodenta Customized Abutment - Titanium
FDA 510(k)
FDA Class 2
·Dental
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 8, 2013
AED PLUS
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·December 13, 2010
COULTER LH 750 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·July 22, 2014