24 results
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35ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FUJI II LC (IMPROVED)
FDA 510(k)
FDA Class 2
·Dental
Bronze SureTrak® II System
FDA UDI
MEDTRONIC NAVIGATION, INC.·00721902672316·SCREWDRIVER 961584 SURETRAK2
N/A
FDA UDI
MEDTRONIC NAVIGATION, INC.·00721902467660·CLAMP DRIVER 961-584 ACC SURETRAK2
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471149830·K-WIRE - DOUBLE TROCAR FULLY THREADED 1.5mm DIA...
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010
TRANSEND GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010
TRANSEND EX 14 GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code DQX·September 23, 2009
GRAM NEGATIVE COMBO PANEL TYPE 3
FDA 510(k)
FDA Class 2
·Microbiology
ASAHI® Peripheral Vascular Guide Wire ASAHI Meister®16
FDA 510(k)
FDA Class 2
·Cardiovascular
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·February 28, 2022
TRANSEND GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 27, 2010
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·October 26, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·August 22, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·November 28, 2023
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·April 18, 2023
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·September 25, 2024
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·October 15, 2025