15 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Celt ACD Vascular Closure Device 6F
FDA UDI
VASORUM LIMITED·05391530280068·Celt ACD Vascular Closure Device 6F
Celt ACD Vascular Closure Device 6F_ESP
FDA UDI
VASORUM LIMITED·05391530280099·Celt ACD Vascular Closure Device 6F_ESP
Celt ACD PLUS Vascular Closure Device 7F
FDA UDI
VASORUM LIMITED·05391530280679·Celt ACD PLUS Vascular Closure Device 7F (US)
Celt ACD PLUS Vascular Closure Device 6F
FDA UDI
VASORUM LIMITED·05391530280648·Celt ACD PLUS Vascular Closure Device 6F (US)
Celt ACD PLUS Vascular Closure Device 5F
FDA UDI
VASORUM LIMITED·05391530280617·Celt ACD PLUS Vascular Closure Device 5F (US).
Celt ACD Vascular Closure Device 5F_ESP
FDA UDI
VASORUM LIMITED·05391530280037·Celt ACD Vascular Closure Device 5F_ESP
Celt ACD Vascular Closure Device 5F
FDA UDI
VASORUM LIMITED·05391530280006·Celt ACD Vascular Closure Device 5F
Celt ACD Vascular Closure Device 7F
FDA UDI
VASORUM LIMITED·05391530280129·Celt ACD Vascular Closure Device 7F
Celt ACD Vascular Closure Device 7F_ESP
FDA UDI
VASORUM LIMITED·05391530280150·Celt ACD Vascular Closure Device 7F_ESP
CELT ACD VASCULAR CLOSURE DEVICE 6F
FDA Adverse Event
Malfunction
·VASORUM LIMITED·Product code MGB·September 16, 2024
CELT ACD VASCULAR CLOSURE DEVICE
FDA Adverse Event
Injury
·VASORUM LTD.·Product code MGB·April 23, 2021
AORTIC EXCLUDER AAA ENDOPROSTHESIS (LOW PERM)
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·January 2, 2019
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·March 1, 2018
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·January 17, 2024
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·February 8, 2024