23 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BD Kiestra IdentifA
FDA 510(k)
FDA Class 2
·Microbiology
BD KIESTRA IDENTIFA
FDA Adverse Event
Malfunction
·BD KIESTRA LAB AUTOMATION·Product code QBN·October 8, 2025
BD KIESTRA¿ IDENTIFA
FDA Adverse Event
Malfunction
·BD KIESTRA LAB AUTOMATION·Product code QBN·December 9, 2024
DTE
FDA UDI
Guilin Woodpecker Medical Instrument Co., Ltd.·06944843657769·Dental X-Ray Device
HYDROCEL VERTEBRAL BODY REPLACEMENT, MODEL 06-172-00XX1
FDA 510(k)
FDA Class 2
·Orthopedic
MYOSURE XL ROD LENS HYSTEROSCOPE, MYOSURE XL OUTLFOW CHANNEL
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·December 2, 2024
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·October 9, 2025
RESOLUTION CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·June 17, 2025
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·November 25, 2024
RESOLUTION CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·January 8, 2025
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·March 6, 2025
RESOLUTION CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·June 11, 2025
RESOLUTION CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·February 13, 2025
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·January 8, 2025
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·March 4, 2025
RESOLUTION CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·March 28, 2025
NEUROFORM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code NJE·November 6, 2008
AUTOMATED PD SET W/CASSETTE4 PRONG
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 25, 2011
2520274-2013-04378
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·July 12, 2013