21 results · 24ms · Sources: EU EUDAMED, US FDA

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WRIGHT RESPIROMETER, MARK 8, AND 14 RESPIROMETER, MODEL 700-021, 700-008, 700-014

FDA 510(k)
FDA Class 2 ·Anesthesiology

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450385746·

SYRINGE MANAGEMENT SYSTEM, MODEL SMS-1

FDA 510(k)
FDA Class 2 ·General Hospital

ABBOTT TUMORMARKER-MCC (LYOPHILIZED), LEVELS 1 AND 2, 2ML NO. 6E21-10

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

SOVEREIGN SPINAL SYSTEM

FDA Adverse Event
Injury ·MSD DEGGENDORF MFG·Product code MAX·December 23, 2014

SOVEREIGN SPINAL SYSTEM

FDA Adverse Event
Injury ·MSD DEGGENDORF MFG·Product code MAX·November 22, 2014

SOVEREIGN SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code OVD·April 21, 2018

SOVEREIGN SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·May 10, 2013

SOVEREIGN SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MDT SWINNEA DC·Product code MAX·February 18, 2011

SOVEREIGN SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code OVD·August 9, 2017

PASSPORT 2 MONITOR

FDA Adverse Event
Malfunction ·MONDRAY DS USA, INC·Product code DSI·April 30, 2013

LAMITRODE S4

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·August 28, 2014

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·May 17, 2011

SOVEREIGN¿ SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·November 15, 2012

SOVEREIGN SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code OVD·November 28, 2017

SOVEREIGN SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code MAX·August 19, 2011

SOVEREIGN SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code OVD·November 30, 2015

SOVEREIGN¿ SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·December 5, 2012

SOVEREIGN¿ SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code OVD·November 18, 2025

INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

FDA Adverse Event
Injury ·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019