41 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DiLumen Endolumenal Interventional Platform
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Disect Gen Surg
FDA UDI
KATENA PRODUCTS, INC.·00841668101049·WRIGHT FASCIA NEEDLE
ILLY NEEDLE
FDA UDI
H.S. HOSPITAL SERVICE SPA·08033055143370·AGO TIPO ILLINOIS 18GX25-40MM
PTFE PORTABLE INTRODUCER
FDA 510(k)
FDA Class 2
·Cardiovascular
GE ENTROPY SENSOR
FDA 510(k)
FDA Class 2
·Neurology
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
NIPRO BLOOD TUBING SET W/TP
FDA Adverse Event
Malfunction
·NIPRO (THAILAND) CORP. LTD.·Product code FJK·February 6, 2024
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 6, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 4, 2021