29 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FASTIN RC ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
Septal splints
FDA UDI
Spiggle & Theis Medizintechnik GmbH·04250381809822·FEP, standard
0.75 m...
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·10304040059989·Acclean Disp Prophy Angle Firm White
AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 75mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665010015·
Septal splints
FDA UDI
Spiggle & Theis Medizintechnik GmbH·04250381809839·FEP, standard
0.75 m...
Arthrex®
FDA UDI
ARTHREX, INC.·00888867522206·Cannulated Canc Screw,36mm Thd,7.0x75mm
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code MNL·October 7, 2015
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ITX·October 7, 2015
BMC COAXIAL INJECTABLE CATHETER, MODEL CIC 38/145 AND CIC 35/145
FDA 510(k)
FDA Class 2
·Cardiovascular
EASYBELL
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
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