52 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Etest Ceftaroline (0.002 - 32ug/ml)
FDA 510(k)
FDA Class 2
·Microbiology
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100226·THORLAKSON ASPIRATING SPECULUM
DISPOSABLE TEMPERATURE, SKIN AND ESOPHAGEAL PROBES
FDA 510(k)
FDA Class 2
·General Hospital
MASTERSCREEN IOS
FDA 510(k)
FDA Class 2
·Anesthesiology
AQUACEL FOAM
FDA Adverse Event
Injury
·CONVATEC INC·Product code NAC·October 6, 2014
7" SMALLBORE PRESSURE INFUSION EXT. SET
FDA Adverse Event
Other
·ICU MEDICAL, INC.·Product code FPA·May 20, 2013
SPEEDBAND SUPERVIEW SUPER 7, MODELS 4205
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code MND·July 6, 2011
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·April 2, 2021
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 9, 2019
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 11, 2024
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 20, 2020
SENRI
FDA Adverse Event
Injury
·KANEKA·Product code LIT·March 12, 2019
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·May 6, 2025
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·December 24, 2025
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2020
18 SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 19, 2025
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2025
18 SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·June 11, 2024