10 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PROMAX SURGICAL DRAPES AND COVERS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DeltaForm HD
FDA UDI
Merz Dental GmbH·D7091980183·DeltaForm HD lower posteriors, L, BL3 -MADE IN ...
WALLSTENT ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code JCT·January 15, 2025
Ritter Dental Implant System
FDA 510(k)
FDA Class 2
·Dental
CONTROL SET DAT I, CONTRL SET DAT II, CONTROL SET DAT III, CONTROL SET AMPHETAMINE 1000 AND CONTROL SET AMPHETAMINE 500
FDA 510(k)
FDA Class 1
·Clinical Toxicology
WALLSTENT ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 22, 2025
WALLSTENT ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 1, 2025
PETITE PACING LEAD
FDA Adverse Event
Malfunction
·OSCOR INC·Product code DTB·February 1, 2013
CYCLER 220 VOLT HOMECHOICE PROAUTOMATED PD
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - LARGO·Product code FKX·February 7, 2011
COMPRESSOR MINI
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code BTI·July 2, 2014