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

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VALLEYLAB E2750 LAPAROSCOPIC HANDSET, VALLEYLAB E2770 SERIES ELECTRODES

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

BOSS Instruments

FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515251434·Freeman Flap Ret, 1" wide, 8"

SPONGE, SURGICAL, GAUZE, COMPRESSED 2 BY 2 INCHES

FDA 510(k)
FDA Unclassified ·Unknown

RAICHEM (TM) SPIA (TM) - ACID GLYCOPROTEIN REAGENT

FDA 510(k)
FDA Class 1 ·Immunology

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 3, 2019

TSRH

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 11, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·February 10, 2017

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·January 9, 2017

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 12, 2020

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 12, 2020

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 22, 2016

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·October 6, 2016

HEARTSTART MRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 22, 2014

COMBI SET TRUE FLOW SERIES BLOOD TUBING -8MM PUMP

FDA Adverse Event
FRESENIUS MEDICAL CARE OF NORTH AMERICA·Product code FJK·February 8, 2013

TOTALCARE

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·December 21, 2010

TSRH

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·October 7, 2011

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 22, 2016

TSRH

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·October 12, 2018

TSRH

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·March 15, 2017

TSRH

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·May 14, 2017