9,596 results
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47ms
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Sources: EU EUDAMED, US FDA
Stryker Neurovascular
Manufacturer
🇺🇸 United States·1 Importer
Stryker Neurovascular
FDA registration
Stryker Neurovascular·9 products·🇺🇸 United States
Stryker Neurovascular
FDA registration
Stryker Neurovascular·17 products·🇺🇸 United States
Stryker Neurovascular
FDA registration
Stryker Neurovascular·10 products·🇮🇪 Ireland
STRYKER NEUROVASCULAR
FDA Adverse Event
Death
·STRYKER NEUROVASCULAR·Product code NJE·April 15, 2019
COIL-HYDRAULIC
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·January 3, 2024
AMPLATZER VASCULAR PLUG
FDA Adverse Event
Injury
·AGA MEDICAL CORPORATION·Product code KRD·September 11, 2018
PIPELINE
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·October 5, 2023
STRYKER NEUROVASCULAR NEUROFORM ATLAS WITHOUT TIP
FDA Adverse Event
Malfunction
·STRYKER NEUROVASCULAR·Product code NJE·August 16, 2022
EXCELSIOR XT-27 STD STRAIGHT 150CM
FDA Adverse Event
Malfunction
·STRYKER NEUROVASCULAR·Product code DQY·August 1, 2024
TARGET XL 360 SOFT 4MM X 12CM
FDA Adverse Event
Malfunction
·STRYKER NEUROVASCULAR CORK·Product code HCG·May 23, 2018
UNKNOWN (SURPASS STREAMLINE)
FDA Adverse Event
Injury
·STRYKER NEUROVASCULAR CORK·Product code OUT·November 26, 2019
STENT - VASCULAR RECONSTRUCTION
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code NJE·March 8, 2022
TARGET XL 360 SOFT 10MM X 40CM
FDA Adverse Event
Malfunction
·STRYKER NEUROVASCULAR CORK·Product code HCG·October 24, 2016
Stryker European Operations Limited
Authorized representative
🇮🇪 Ireland·16 Manufacturers
TARGET XL 360 SOFT 6MM X 20CM
FDA Adverse Event
Malfunction
·STRYKER NEUROVASCULAR CORK·Product code HCG·November 21, 2016
TARGET XL HELICAL 5MM X 15CM
FDA Adverse Event
Malfunction
·STRYKER NEUROVASCULAR CORK·Product code HCG·November 21, 2016
NEUROFORM ATLAS 3.0MM X 24MM NO TIP - CE
FDA Adverse Event
Malfunction
·STRYKER NEUROVASCULAR CORK·Product code QCA·November 6, 2024
LVIS
FDA Adverse Event
Injury
·MICROVENTION, INC.·Product code QCA·May 8, 2025
UNKNOWN ENVOY 6F
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code DQY·August 12, 2016