20 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EXHALATION VALVE
FDA 510(k)
FDA Class 2
·Anesthesiology
NexxZr™ T / D-100-35-NT-C400-SD
FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271113535·
LIQUID OXYGEN SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
SUSPENSION ACROMIOCLAVICULAR (AC) REPAIR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
UV PHOTOTHERAPY
FDA Adverse Event
Injury
·UNK·Product code FTC·January 27, 2021
UV PHOTOTHERAPY
FDA Adverse Event
Injury
·XUZHOU KERNEL MEDICAL INSTRUMENT EQUIPMENT CO.·Product code FTC·November 30, 2022
WAVEWRITER ALPHA?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·March 24, 2026
UV PHOTOTHERAPY
FDA Adverse Event
Injury
·UNK·Product code FTC·January 25, 2021
UV PHOTOTHERAPY LAMP
FDA Adverse Event
Injury
·ANGEL KISS LLC.·Product code FTC·February 3, 2021
UV PHOTOTHERAPY
FDA Adverse Event
Injury
·UNK·Product code FTC·January 26, 2021
UV PHOTOTHERAPY LAMP
FDA Adverse Event
Injury
·UNK·Product code FTC·January 29, 2021
UV PHOTOTHERAPY
FDA Adverse Event
Injury
·ANGEL KISS LLC·Product code FTC·February 2, 2021
UV PHOTOTHERAPY LAMP
FDA Adverse Event
Injury
·ANGEL KISS LLC.·Product code FTC·February 4, 2021
MAXZERO NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·January 6, 2020
ETRIO
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GEI·May 29, 2013
560 BIO-CONSOLE BASE UNIT
FDA Adverse Event
Injury
·MEDTRONIC PERFUSION SYSTEMS·Product code DWA·June 10, 2011
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES·Product code MIH·August 22, 2008
MAXZERO NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·September 2, 2020
MAXZERO NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·May 8, 2020
MAXZERO NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·May 8, 2020