23 results · 25ms · Sources: EU EUDAMED, US FDA

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ENDOGASTRIC STOMAPHYX DEVICE AND ACCESSORIES

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496062875·SOCKS FOR YOU BAMBOO OPERA, SIZE XXL, BORDEAUX,...

SIGNA OPENSPEED MAGNETIC RESONANCE SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

MODIFICATION TO BD VACUTAINER PUSH BUTTON BLOOD COLLECTION SET

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·January 12, 2016

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 23, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 23, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 22, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 23, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 23, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·April 16, 2018

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 1, 2013

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 1, 2013

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·February 14, 2018

DIEGO FOOTSWITCH

FDA Adverse Event
Injury ·GYRUS ACMI, INC.·Product code ERL·April 12, 2013

LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM

FDA Adverse Event
Malfunction ·ALLERGAN·Product code LTI·March 18, 2011

PRECISE RX NITINOL STENT

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code NIM·June 18, 2008

STONEBREAKER SINGLE USE PROBE

FDA Adverse Event
Malfunction ·COOK INC·Product code FFK·March 28, 2018

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·January 9, 2018

CALCIUM

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES (IRVING IA/CC)·Product code CJY·September 1, 2020