7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BONE MULCH SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
1505 P102,FB,NURSE ONLY,WHITE,STKR
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828146272·1505 P102,FB,NURSE ONLY,WHITE,STKR
LUBREASE FEMALE LUBRICANT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
i-STAT CHEM8+ cartridge with the i-STAT 1 System
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·March 6, 2013
CONSULTA
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·February 15, 2011
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·August 8, 2014