65 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Portable ECG Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
ENTERAL ADMINISTRATION SET WITH SOLUTION CONTAINER, ENTERAL ADMINISTRATION SET, ENTERAL EXTENSION SET WITH MINITUBE CONN
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
RAPHAEL COLOR
FDA 510(k)
FDA Class 2
·Anesthesiology
WALLSTENT RP ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MAF·April 19, 2023
DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) PACEMAKER ELECTRODE
FDA Adverse Event
Injury
·MPRI·Product code OJX·June 8, 2013
COLLEAGUE PRE 1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011
AXSYM RUBELLA IGG ANTIBODY
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code LFX·September 10, 2008
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
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 20, 2020
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 25, 2024
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
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024