17 results
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53ms
·
Sources: EU EUDAMED, US FDA
USA Therm Inc.
FDA registration
USA Therm Inc.·1 product·🇺🇸 United States
ThermPix
FDA UDI
USA THERM, INC.·00860008801906·The ThermPix® Thermovisual Camera is intended t...
ERBE VIO 3
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·March 7, 2024
ERBE VIO 300D
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·November 20, 2015
ERBE VIO 3
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·March 16, 2026
ERBE VIO 200 S
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·February 2, 2023
ERBE VIO 200 S
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·May 11, 2023
ERBE ICC 200 E/A
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·February 26, 2024
ARTIC SUN 5000, 115V NA
FDA Adverse Event
Injury
·DYMAX CORP. -2523003·Product code DWJ·July 7, 2017
ERBE VIO 300 D
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·February 5, 2020
SOFTHEAT
FDA Adverse Event
Injury
·KAZ USA, INC.·Product code IRT·June 22, 2015
ERBE VIO 300 D
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·August 1, 2023
ERBE APC FILTER INTEGRATED SIDE FIRE PROBE
FDA Adverse Event
Malfunction
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·July 14, 2022
ERBE VIO 200 D
FDA Adverse Event
Death
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·January 3, 2024
ERBE VIO DV
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·October 17, 2024
ERBE ICC 200 E/A
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·January 19, 2018
SOFTHEAT
FDA Adverse Event
Injury
·KAZ USA, INC.·Product code IRT·October 7, 2015