10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Megapulse III Shortwave Diathermy
FDA 510(k)
FDA Class 2
·Physical Medicine
READY VIEW
FDA 510(k)
FDA Class 2
·Radiology
THE SENSITITRE AIM
FDA 510(k)
FDA Class 2
·Microbiology
ATTUNE PS FEM LT SZ 8 CEM
FDA Adverse Event
Malfunction
·DEPUY IRELAND - 9616671·Product code OIY·March 23, 2021
DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code PQF·December 7, 2018
VIRTUOSO DR
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code LWS·June 8, 2013
NA
FDA Adverse Event
Malfunction
·STRYKER SUSTAINABILITY SOLUTIONS LAKELAND·Product code NUJ·October 8, 2014
SYNERGY
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·June 21, 2011
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 22, 2022
ELEKTA LIMITED Versa HD, REF XRT 2121, 2131; Medical Charged-Particle Radiation Therapy System Accelerator, Linear
FDA Enforcement
Class II
·Ongoing·Elekta, Inc.·December 13, 2023