8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LDE4 Lancing Device
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LCP
FDA UDI
Synthes GmbH·10886982157287·4.5MM LCP® CONDYLAR PLATE 6 HOLES/170MM-RIGHT
SENSITITRE 18-24 HOURS SUSCEPTIBILITY PLATES
FDA 510(k)
FDA Class 2
·Microbiology
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, YELLOW COLOR
FDA 510(k)
FDA Class 1
·General Hospital
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·September 3, 2024
BHR
FDA Adverse Event
Injury
·SMITH & NEPHEW·Product code NXT·November 4, 2014
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·August 25, 2011
M2A 38MMX52MM CUP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·July 12, 2013