20 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MicroScan Dried Gram Negative MIC/Combo Panels with Ciprofloxacin (Cp) (0.004 - 8µg/mL)
FDA 510(k)
FDA Class 2
·Microbiology
AGXO
FDA UDI
Oticon A/S·05707131342706·G200, MINIRITE T 312 2.4G C063 AGXO
IBED WIRELESS WITH IBED AWARENESS
FDA 510(k)
FDA Class 2
·General Hospital
MASTERKA 40 MASTERKA 35 MASTERKA 30
FDA 510(k)
FDA Unclassified
·Unknown
BD SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·July 9, 2025
BD SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·June 7, 2025
BD SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·June 7, 2025
BD SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·June 7, 2025
BD SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·June 7, 2025
BD SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·June 7, 2025
BD SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·June 7, 2025
BD SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·June 7, 2025
BD SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·June 7, 2025
BD SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·June 6, 2025
BD SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·June 6, 2025
TENDRIL SDX
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC CRMD·Product code DTB·January 13, 2014
HILL-ROM LIKO GOLVO LIFT
FDA Adverse Event
Injury
·LIKO AB·Product code FSA·June 20, 2013
GYNECARE MESH UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·October 31, 2015
BD PRECISIONGLIDE¿ 27 G X 1/2" HYPODERMIC NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·March 8, 2023
HEARTWARE® VENTRICULAR ASSIST SYSTEM - BATTERY
FDA Adverse Event
Malfunction
·HEARTWARE·Product code DSQ·October 6, 2017