46 results · 30ms · Sources: EU EUDAMED, US FDA

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SYSMEX XE-5000

FDA 510(k)
FDA Class 2 ·Hematology

APPLIANCE, FIXATION, SPINAL INTERLAMINAL

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·October 25, 2017

BD PRE-FILLED HEPARIN LOCK FLUSH IN 0.9% SODIUM CHLORIDE INJECTION, USP SYRINGE

FDA 510(k)
FDA Class 2 ·General Hospital

PVP-POLYVINYLPYRROLIDONE REAGENT, MODEL CAT#2210

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

TSRH SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·August 3, 2020

TSRH SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·May 11, 2020

TSRH SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code NKB·February 3, 2010

TSRH SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code NKB·February 3, 2010

ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NKB·December 22, 2017

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 26, 2019

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 26, 2018

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 2, 2019

AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code FNL·April 22, 2013

SECURE II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·April 19, 2011

SIGMA 300 SR

FDA Adverse Event
Injury ·MEDTRONIC S.A.·Product code DXY·July 10, 2008

TSRH SPINAL SYSTEM

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

TSRH SPINAL SYSTEM

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

UNK - SCREW

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code KWQ·July 26, 2011

UNK - SCREW

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code KWQ·July 26, 2011