52 results · 23ms · Sources: EU EUDAMED, 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