59 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AUTOMATED ENDOSCOPE LEAK TESTER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
UniTip Catheter
FDA UDI
Unisensor AG·07640172973547·
KSEA SCB ACC CONTROL
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
REMOTELY CONTROLLED MANDIBULAR POSITIONER, RCMP
FDA 510(k)
FDA Class 2
·Dental
NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026
ARCHITECT HAVAB-IGG
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·May 8, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 23, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 19, 2026
ARCHITECT HAVAB-IGG
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·April 3, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 19, 2026
HUDSON ADULT HEATED WIRE CIRCUIT DUAL LIMB
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAI·May 14, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·September 26, 2014
2210968-2011-00656
FDA Adverse Event
Malfunction
·ETHICON INC.-GMBH·June 14, 2011
STYLE 68 SALINE FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·Product code FWM·July 7, 2021
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 19, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 19, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 19, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 19, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 19, 2026