1,228 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749124712·Treede Maxposition Blade 46x30mm, D40
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749041101·Morse sternotomy retract. 180x275 mm, cur.bl. 4...
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749041088·Morse sternotomy retract. 154x255mm, curv.bl.19...
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749120134·Treede Maxposition Blade 46x40mm, D60
Z-MED
FDA Adverse Event
Death
·B. BRAUN·Product code OZT·August 12, 2023
Z-MED
FDA Adverse Event
Malfunction
·B. BRAUN·Product code OZT·August 12, 2023
KII SLEEVE
FDA Adverse Event
Malfunction
·APPLIED MEDICAL RESOURCES·Product code GCJ·July 26, 2024
EDISON SYSTEM
FDA Adverse Event
Death
·HISTOSONICS, INC.·Product code QGM·May 8, 2025
EDWARDS ESHEATH+ INTRODUCER SET
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES LLC·Product code DYB·October 17, 2025
EDWARDS EXPANDABLE SHEATH INTRODUCER
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·March 23, 2018
Z-MED II
FDA Adverse Event
Malfunction
·B. BRAUN·Product code OZT·August 12, 2023
KII 12 X 100 Z-THREADED OPT SEP SYSTEM
FDA Adverse Event
APPLIED MEDICAL·Product code GCJ·September 9, 2011
ENDURANT ABDOMINAL STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC, GALWAY·Product code MIH·January 4, 2012
ZMED II
FDA Adverse Event
Malfunction
·B BRAUN MEDICAL, INC. MANUFACTURING DIVISION·Product code LIT·January 26, 2006
UROMAT 3000
FDA Adverse Event
Malfunction
·PAUSCH LLC·Product code MMZ·April 22, 2010
LITHOSTAR MODULARIS
FDA Adverse Event
Injury
·SIEMENS AG·Product code MMZ·December 10, 2012
IDI
FDA Adverse Event
Injury
·IMAGE DIAGNOSTICS, INC.·Product code MMZ·July 15, 2021
LITHOSTAR MODULARIS
FDA Adverse Event
Injury
·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code MMZ·December 11, 2009
LITHOSTAR MODULARIS
FDA Adverse Event
Injury
·SIEMENS AG·Product code MMZ·April 8, 2005
SONESTA
FDA Adverse Event
Malfunction
·STILLE-SONESTA INC·Product code MMZ·April 8, 2005