166 results · 39ms · Sources: EU EUDAMED, US FDA

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Vasorum Ltd.

Manufacturer
🇮🇪 Ireland

CELT ACD PLUS VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·December 16, 2025

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·June 17, 2024

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·March 27, 2023

CELT ACD PLUS VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·June 11, 2025

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·October 16, 2025

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·April 17, 2025

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·August 13, 2021

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·March 27, 2023

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Malfunction ·VASORUM LTD.·Product code MGB·July 30, 2024

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·December 3, 2024

CELT ACD PLUS VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·May 22, 2025

CELT ACD VASCULAR DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·November 27, 2025

CELT ACD PLUS VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·September 19, 2025

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·April 8, 2025

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD.·Product code MGB·February 12, 2025

CELT ACD PLUS VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD·Product code MGB·May 8, 2026

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD·Product code MGB·March 24, 2026

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Injury ·VASORUM LTD·Product code MGB·June 12, 2019

CELT ACD VASCULAR CLOSURE DEVICE

FDA Adverse Event
Malfunction ·VASORUM LTD.·Product code MGB·April 17, 2024