24 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TALOS-C CERVICAL INTERVERTEBRAL BODY FUSION DEVICES
FDA 510(k)
FDA Class 2
·Orthopedic
RUSCH
FDA UDI
TELEFLEX INCORPORATED·54026704624558·RUSCH Traditional Guedel Airway Length 50mm Tra...
EagleBoard™ MR
FDA UDI
MACROMEDICS B.V.·08719425704159·EagleBoard, 3P, MR Safe (base only)
ELMED
FDA UDI
ELMED INCORPORATED·00842180194359·Tubing clamp forceps. Heavier, with deep serrat...
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970546·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970553·
Typhoon(TM) Facet Screw Fixation System
FDA 510(k)
FDA Unclassified
·Unknown
TARGET DETACHABLE COIL
FDA 510(k)
FDA Class 2
·Neurology
NIOX
FDA UDI
Circassia AB·07350047030700·Contains one sensor preprogrammed for a defined...
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·October 15, 2025
STANMORE COCR FMRL SZ3 STD
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·December 29, 2017
ULTRASONIC IMAGING CATHETER - CORONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code DQO·May 21, 2013
PINN MAR +4 10D 36IDX58OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 3, 2011
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·August 14, 2008
28MM DIAMETER COBALT CHROMIUM MODULAR HEAD -6MM NECK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·May 25, 2018
ALINITY I HAVAB IGG REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·November 26, 2025
ALINITY I HAVAB IGG REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·July 22, 2025
ALINITY I HAVAB-IGG REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·June 25, 2025
ALINITY I HAVAB-IGG REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·June 25, 2025
ALINITY I HAVAB IGG REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·January 23, 2026