747 results · 23ms · Sources: EU EUDAMED, US FDA

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Penumbra System 110 Aspiration Tubing

FDA 510(k)
FDA Class 2 ·Cardiovascular

PENUMBRA SYSTEM MAX ASPIRATION TUBING

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·June 24, 2015

Masel

FDA UDI
Ortho Organizers, Inc.·00190707040932·Choice™ Torquing Pliers - Male

ProLift

FDA UDI
Life Spine, Inc.·00190837105884·Static Expandable Cage Trial, 12mm x 28mm x 7mm...

ANATOMICAL SHOULDER KEELED GLENOID

FDA 510(k)
FDA Class 2 ·Orthopedic

INQUIRY AFOCUSII DIAGNOSTIC CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 12, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 11, 2024

BIPAP A40

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 9, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 6, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 13, 2024

TBD

FDA Adverse Event
Injury ·MPRI·Product code LWP·June 7, 2013

UNICEL DXC 800 SYNCHRON SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 24, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·September 10, 2008

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 16, 2024

BIPAP A40 PRO, IT

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 5, 2025

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·June 5, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·June 6, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·June 5, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 11, 2024