335 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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Préime DermaFacial (MicroT)
FDA 510(k)
FDA Class 2
·Neurology
Oph. Cystotomes
FDA UDI
KATENA PRODUCTS, INC.·00841668113721·CYSTOTOME CURVED 27GA
BECTON DICKINSON
FDA registration
BECTON DICKINSON·52 products·🇺🇸 United States
BD NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMI·May 28, 2026
GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS
FDA 510(k)
FDA Class 1
·Microbiology
ENROUTE Transcarotid Neuroprotection System
FDA 510(k)
FDA Class 2
·Cardiovascular
BD PLASTIPAK SYRINGES
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code FMF·March 15, 2013
BD PLASTIPAK SYRINGES
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code FMF·March 15, 2013
BD PLASTIPAK SYRINGES
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code FMF·March 15, 2013
BD PLASTIPAK SYRINGES
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code FMF·March 15, 2013
ECLIPSE LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·March 30, 2026
VENFLON 2 BL 22GA IV CANNULA
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FOZ·December 24, 2020
BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE
FDA Adverse Event
Malfunction
·BD CARIBE LTD.·Product code JKA·February 12, 2025
BD¿ SHARPS COLLECTOR
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·June 16, 2023
2243072-2017-00211
FDA Adverse Event
Malfunction
·October 27, 2017
2243072-2017-00238
FDA Adverse Event
Malfunction
·December 1, 2017
2243072-2017-00228
FDA Adverse Event
Injury
·December 1, 2017
2243072-2017-00209
FDA Adverse Event
Malfunction
·October 31, 2017
2243072-2017-00413
FDA Adverse Event
Malfunction
·December 28, 2017
2243072-2017-00197
FDA Adverse Event
Malfunction
·October 30, 2017