16 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Clean Connecting Tube
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INTROCAN SAFETY IV CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
OMNI 3 OXYGEN SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
INTROCAN SAFETY®
FDA Adverse Event
Injury
·B BRAUN MELSUNGEN AG·Product code FOZ·April 1, 2025
UNK DY
FDA Adverse Event
Malfunction
·COVIDIEN·Product code MPB·October 31, 2008
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·August 23, 2011
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORPORATION·Product code LLZ·July 8, 2013
BD INTIMA II¿ IV CATHETER PRN ADAPTER
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·July 6, 2023
INTROCAN SAFETY®
FDA Adverse Event
Injury
·B BRAUN MELSUNGEN AG·Product code FOZ·August 11, 2025
INTROCAN SAFETY®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·March 20, 2025
BIOABSORBABLE INTERFERENCE SCREWS
FDA Adverse Event
Malfunction
·S.B.M. SAS·Product code MAI·August 22, 2024
VERRATA PLUS PRESSURE GUIDE WIRE
FDA Adverse Event
Malfunction
·VOLCANO CORPORATION·Product code DQX·November 24, 2018
GREENLIGHT ADDSTAT
FDA Adverse Event
Malfunction
·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·September 13, 2010
INTROCAN SAFETY®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·October 2, 2025
INTROCAN SAFETY®
FDA Adverse Event
Injury
·B BRAUN MELSUNGEN AG·Product code FOZ·April 10, 2025
Model Number L111, ESSENTIO DR SL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025