48 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CODMAN BACTISEAL CATHETERS, CODMAN BACTISEAL EVD CATHETER
FDA 510(k)
FDA Class 2
·Neurology
OPTI-FREE EXPRESS MULTI-PURPOSE DISINFECTING SOLUTION
FDA 510(k)
FDA Class 2
·Ophthalmic
FAST SET PUTTY
FDA 510(k)
FDA Class 2
·Neurology
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970072·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970102·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970089·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970119·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970096·
C-SECTION TRAY PACK
FDA Adverse Event
Injury
·MEDLINE INDUSTRIES, LP·Product code LRO·October 28, 2025
PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 31, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 30, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 20, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 8, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 20, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 23, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 29, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 24, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 27, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 22, 2026