39 results · 21ms · Sources: EU EUDAMED, US FDA

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BAROSENSE ENDOGASTRIC TUBE (EGT), MODEL F0034

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

OPTI-FREE EXPRESS MULTI-PURPOSE DISINFECTING SOLUTION

FDA 510(k)
FDA Class 2 ·Ophthalmic

FAST SET PUTTY

FDA 510(k)
FDA Class 2 ·Neurology

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

CMF CUSTOMIZED IMPLANT KIT LARGE

FDA Adverse Event
Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KKY·March 7, 2013

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 22, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 15, 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 16, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 15, 2026

IMP,TSV,4.1MM,SBM,13

FDA Adverse Event
Injury ·ZIMVIE US CORP LLC·Product code DZE·October 21, 2025