87 results
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28ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ORTHOPEDIATRICS PEDIPLATES SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
General Instrument
FDA UDI
ALPHATEC SPINE, INC.·00840180505533·TLIF Shavers
LATEX POWDER-FREE EXAMINATION GLOVES BLUE, POLYMER COATED, CONTAINS 50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTABLE PRO
FDA 510(k)
FDA Class 1
·General Hospital
SURGITRON IEC II
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
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
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 7, 2025
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
DUO FLUID CART
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·December 21, 2017
ARTIS ZEEGO III (CHINA)
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·December 26, 2023
ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·August 31, 2018
TALENT TAA
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·April 26, 2013
RESTORE PRIME ADVANCED
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·April 22, 2011
ALARIS SYSTEM PUMP MODULE
FDA Adverse Event
Death
·CARDINAL HEALTH ALARIS PRODUCTS·Product code FRN·July 25, 2008
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·October 28, 2025
ULTRAFLEX DUO HIGH FLUID CART - REFURBISHED
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·June 25, 2020
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