10,000 results
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59ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARTERIAL EMBOLIZATION DEVICE (KRD)
FDA 510(k)
FDA Class 2
·Cardiovascular
KRD PL 2000 CONTROLLED PASSIVE MOTION (CPM) PORTABLE
FDA 510(k)
FDA Class 1
·Physical Medicine
HCG, KRD
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code HCG·August 4, 2020
DIGITAL RAIOGRAPHIC KRD
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS·Product code IZO·January 9, 2006
KRD DEVICE, EMBOLIZATION, VASCULAR
FDA Adverse Event
Injury
·COOK INC·Product code KRD·July 16, 2024
KRD DEVICE, EMBOLIZATION, VASCULAR
FDA Adverse Event
Injury
·COOK INC·Product code KRD·July 16, 2024
KRD DEVICE, EMBOLIZATION, VASCULAR
FDA Adverse Event
Injury
·COOK INC·Product code KRD·July 16, 2024
KRD DEVICE, EMBOLIZATION, VASCULAR
FDA Adverse Event
Injury
·COOK INC·Product code KRD·July 16, 2024
KRD DEVICE, EMBOLIZATION, VASCULAR
FDA Adverse Event
Injury
·COOK INC·Product code KRD·August 22, 2023
KRD DEVICE, EMBOLIZATION, VASCULAR
FDA Adverse Event
Injury
·COOK INC·Product code KRD·March 7, 2018
KRD DEVICE, EMBOLIZATION, VASCULAR
FDA Adverse Event
Death
·COOK INC·Product code KRD·February 23, 2018
KRD DEVICE, EMBOLIZATION, VASCULAR
FDA Adverse Event
Injury
·COOK INC·Product code KRD·July 14, 2019
KRD DEVICE, EMBOLIZATION, VASCULAR
FDA Adverse Event
Injury
·COOK INC·Product code KRD·November 27, 2019
KRD DEVICE, EMBOLIZATION, VASCULAR
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·September 19, 2019
KRD DEVICE, VASCULAR, FOR PROMOTING EMBOLIZATION
FDA Adverse Event
Death
·COOK INC·Product code KRD·December 3, 2025
CEREPAKTM
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code KRD·December 27, 2024
DELTAXSFT10 2MM X 6CM
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code KRD·August 15, 2019
CATERPILLAR EMBOLIZATION SYSTEM
FDA Adverse Event
Malfunction
·CLEARSTREAM TECHNOLOGIES LTD.·Product code KRD·October 30, 2020
ORBIT GALAXY DETACHABLE COIL SYSTEM
FDA Adverse Event
Malfunction
·CODMAN SHURTLEFF INC.·Product code HCG·May 31, 2017
GALAXY G3 MINI 1.5MM X 4CM
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code KRD·November 1, 2019