17 results
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24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VELASHAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ULTRA-HIGH ENERGY GENERAL PURPOSE COLLIMATOR (UHGP) [FOR CARDIAC IMAGING]
FDA 510(k)
FDA Class 2
·Radiology
I.V. SET-LUER LOCK WITH LATEX FREE INJECTION SITE, MODEL B411
FDA 510(k)
FDA Class 2
·General Hospital
INFINION CX
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 14, 2021
WAVEWRITER ALPHA PRIME
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 19, 2023
10MM/130 DEG TI CANN TROCH FIXATION NAIL 170MM
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code HSB·April 22, 2013
ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLE
FDA Adverse Event
Injury
·COVIDIEN SURGICAL SUPPLY·Product code GAA·April 21, 2011
GEN2 ADJUSTABLE GASTRIC BAND - 11 CM, UNLOCKA
FDA Adverse Event
Malfunction
·OBTECH MEDICAL SARL·Product code LTI·July 9, 2008
CAPIOX FX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·May 22, 2025
CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 5, 2022
CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 16, 2022
CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·May 24, 2022
CAPIOX FX05 OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DTZ·May 19, 2023
CAPIOX FX25 OXYGENATOR
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 11, 2022
CAPIOX FX25 OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 11, 2022
CAPIOX FX25 OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 29, 2022
CAPIOX FX25 OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·February 14, 2022