41 results · 20ms · Sources: EU EUDAMED, 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