54 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RECON system
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526768512·GENUMEDI PSS GREEN VII
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100394·MURDOCH EYE SPECULUM #3
ProLift Trial
FDA UDI
Life Spine, Inc.·00190837087494·
ALPHA HISTOPLASMA ANTIGEN EIA MODEL HAG102
FDA 510(k)
FDA Class 2
·Microbiology
LEGEND ALL-POLY CUP
FDA 510(k)
FDA Class 2
·Orthopedic
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·May 17, 2024
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·December 3, 2024
ARTIS Q ZEEGO
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·September 29, 2025
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·April 29, 2026
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·April 1, 2026
ARTIS ZEEGO III (CHINA)
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·December 26, 2023
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·July 6, 2011
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 7, 2013
ONE TOUCH ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·September 4, 2008
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·October 28, 2025
ARTIS ZEE III FLOOR
FDA Adverse Event
Malfunction
·SIEMENS AG·Product code OWB·September 10, 2024
ARTIS ZEE III FLOOR
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·July 12, 2024
ARTIS Q ZEEGO (CHINA)
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·May 10, 2024
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·July 12, 2024