54 results · 31ms · Sources: EU EUDAMED, 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