8 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INTERFACE - CAVITY LINER
FDA 510(k)
FDA Class 2
·Dental
LEONE SPA
FDA UDI
LEONE SPA·08033707085423·WEB I MOL BANDS G8424-17+G2820-00 LL 30
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756739405·CRANIOFACIAL BASIC PACK
PATIENT EXAMINATION GLOVES (LATEX)
FDA 510(k)
FDA Class 1
·General Hospital
LIGHT-TOUCH LAPAROSCOPIC MODEL 905200 FIBEROPTIC
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·May 21, 2014
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·January 4, 2013
SYNCHRON® LX20 PRO ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·November 11, 2010