66 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Oryum and Ovem Epidermal Deri Prick Test Applicator
FDA 510(k)
FDA Class 2
·General Hospital
Oticon
FDA UDI
Oticon A/S·05707131334510·OPN 2, KIT 312 2.4G NFM 90 R C001
SENTINEL, MODEL SP-001
FDA 510(k)
FDA Class 2
·Radiology
ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
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
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
BALL HEADS: MECTACER 01.29.209 BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 36 SIZE M
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·December 6, 2023