28 results · 33ms · Sources: EU EUDAMED, US FDA

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BABY POD

FDA 510(k)
FDA Class 1 ·General Hospital

Tornier Latitude

FDA UDI
TORNIER, INC.·00846832020171·ULNAR STEM TRIAL

Symmetry Surgical

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482050996·Symmetry® Scissors, Operating, Straight, Blunt/...

SIMPLICITY WITH WINGS INFUSION SET, (MODEL MMT-103)

FDA 510(k)
FDA Class 2 ·General Hospital

THERASEED(R) PALLADIUM-103 IMPLANT; MODEL 200

FDA 510(k)
FDA Class 2 ·Radiology

TRIAGE CARDIAC TRIPLE MARKER PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 12, 2018

TRIAGE CARDIAC HS PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 22, 2019

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017

TRIAGE CARDIAC TRIPLE MARKER PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code MMI·May 18, 2018

TSRH

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·May 12, 2017

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 2, 2018

TRIAGE CARDIAC PANEL KIT

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code JHX·April 18, 2018

TRIAGE CARDIAC HS PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 21, 2019

TRIAGE CARDIAC TRIPLE MARKER PANEL

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code MMI·October 5, 2017

GRANUFLO

FDA Adverse Event
Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·March 28, 2013

M SERIES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 21, 2011

HARMONIC ACE 36 CM

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·April 15, 2008

TRIAGE CARDIAC TRIPLE MARKER PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·November 1, 2018