11 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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V8 Diagnostic Ultrasound System, V7 Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
Ambler Surgical
FDA UDI
AMBLER SURGICAL CORP.·00190660194802·Corneal trephine blade, short, 8.0mm length, 9....
BD ALCOHOL SWABS
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code LKB·April 29, 2020
CS 8100 CS 8100 ACCESS
FDA 510(k)
FDA Class 2
·Dental
Sonicaid Team3 Antepartum, Sonicaid Team3 Intrapartum
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 13, 2025
TAXUS (R) LIBERTÉ (R)
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·August 23, 2011
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 3, 2014
URETEX SUPPORT PP KIT X1
FDA Adverse Event
Malfunction
·SOFRADIM PRODUCTION·Product code OTN·July 3, 2013
LIFE SCOPE PT
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·December 26, 2023
LIFE SCOPE PT
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·December 8, 2023