28 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DATASCOPE 7.5FR. IAB CATHETER AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Cardiovascular
LINEAR 7.5 FR. 25CC IAB
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - FAIRFIELD·Product code DSP·October 17, 2019
LINEAR 7.5 FR. 25CC IAB
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - FAIRFIELD·Product code DSP·October 17, 2019
LINEAR 7.5 FR. 40CC IAB
FDA Adverse Event
Injury
·DATASCOPE CORP. - FAIRFIELD·Product code DSP·May 14, 2020
GERATHERM BABYWATCH TEMPERATURE MONITOR
FDA 510(k)
FDA Class 2
·General Hospital
INTUITIVE SURGICAL ULTRASONIC SHEARS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118724·TLIF, 28mm X 10mm X 10mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118700·TLIF, 28mm X 10mm X 8mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118762·TLIF, 28mm X 10mm X 14mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118717·TLIF, 28mm X 10mm X 9mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118694·TLIF, 28mm X 10mm X 7mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118731·TLIF, 28mm X 10mm X 11mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118779·TLIF, 28mm X 10mm X 15mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118786·TLIF, 28mm X 10mm X 16mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118755·TLIF, 28mm X 10mm X 13mm, Convex 5°, PEEK
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523118748·TLIF, 28mm X 10mm X 12mm, Convex 5°, PEEK
TSRH® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·April 19, 2013
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC ORTHOPEDIC INC.·Product code KWP·December 4, 2009
BD VENFLON IV CANNULA 20G
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FOZ·July 25, 2023
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWP·December 4, 2009