36 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DIGORA OPTIME (OR DIGORA ONTIME)
FDA 510(k)
FDA Class 2
·Dental
Septal splints
FDA UDI
Spiggle & Theis Medizintechnik GmbH·04250381809808·FEP, standard
0.5 mm...
Arthrex®
FDA UDI
ARTHREX, INC.·00888867522152·Cannulated Canc Screw,36mm Thd,7.0x50mm
AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 50mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665009965·
Septal splints
FDA UDI
Spiggle & Theis Medizintechnik GmbH·04250381809815·FEP, standard
0.5 mm...
Persona® Knee System
FDA UDI
Zimmer, Inc.·00889024656260·
Persona® Knee System
FDA UDI
Zimmer, Inc.·00889024656253·
PERSONA™
FDA UDI
Zimmer, Inc.·00889024459380·
PERSONA™
FDA UDI
Zimmer, Inc.·00889024459397·
MICROSTREAM ORAL NASAL CANNULA FILTERLINE
FDA 510(k)
FDA Class 2
·Anesthesiology
CALCIJECT
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