24 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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H1
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
FlexiNylon cartridges Standard Pink
FDA UDI
PERFLEX LTD·07290110500528·box of 6 identical cartridges sealed in a vacuu...
Cardiovascular Procedure Kit
FDA UDI
Terumo Cardiovascular Systems Corporation·00699753512320·
FlexiNylon cartridges Standard Pink
FDA UDI
PERFLEX LTD·07290110506469·5 identical cartridges sealed in a vacuum bag ;...
IDI-STREP B ASSAY
FDA 510(k)
FDA Class 1
·Microbiology
FEMORAL HEADS, 2.5 AND 7.5 MM NECK LENGTH
FDA 510(k)
FDA Class 2
·Orthopedic
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·December 2, 2024
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·October 9, 2025
SILENT NITE 3D
FDA Adverse Event
Malfunction
·PRISMATIK DENTALCRAFT, INC·Product code LRK·December 10, 2024
RESOLUTION CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·June 17, 2025
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·November 25, 2024
RESOLUTION CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·January 8, 2025
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·March 6, 2025
RESOLUTION CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·June 11, 2025
RESOLUTION CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·February 13, 2025
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·January 8, 2025
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·March 4, 2025
RESOLUTION CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·March 28, 2025
S-ROM M HEAD 36MM +3
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code JDI·November 5, 2008
PROSTAR XL SUTURE-MEDIATED CLOSURE
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·August 25, 2011