28 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RAICHEM CALCIUM (OCPC) LIQUID REAGENT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Humeral Cup Stability
FDA UDI
FX SOLUTIONS·03701037308066·STABILITY TRIAL CUP Ø40 +9
POSTERIOR DISTAL TIBIA PLATE , LEFT
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665024876·
Humeral Cup Stability
FDA UDI
FX SOLUTIONS·03701037309469·HUMERAL CUP STABILITY PE/TA6V Ø40/+9
LEONE SPA
FDA UDI
LEONE SPA·08033707002086·CHROMIUM-COBALT WIRE 0,9mm
RANDOX C-REACTIVE PROTEIN
FDA 510(k)
FDA Class 2
·Immunology
WHITE MTA MATERIAL
FDA 510(k)
FDA Class 2
·Dental
9616026-2006-00240
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
9616026-2006-00244
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
9616026-2006-00239
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
9616026-2006-00222
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
9616026-2006-00252
FDA Adverse Event
Other
·Product code FII·June 21, 2006
9616026-2006-00245
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
9616026-2006-00253
FDA Adverse Event
Other
·Product code FII·June 21, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
9616026-2006-00221
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
PRISMAFLEX SETS (M)
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code KDI·May 13, 2024