16 results · 27ms · Sources: EU EUDAMED, US FDA

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RUSCH REINFORCED TRACHAEL TUBE CUFFED, STERILE

FDA 510(k)
FDA Class 2 ·Anesthesiology

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·14026704921949·

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704286908·LUMBAR LAMINA SPREADER #1 3 1/2"

DESERET POSITIONAL SUTURE WING

FDA 510(k)
FDA Class 1 ·General Hospital

HYSTEROMAT HYSTEROFLATOR HYSTEROSCOPIC INSUFFLATOR

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

BAERVELDT SHUNT

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

BAERVELDT SHUNT

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

BAERVELDT SHUNT

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

BAERVELDT SHUNT

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

BAERVELDT SHUNT

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 5, 2012

BAERVELDT SHUNT

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 5, 2012

BAERVELDT SHUNT

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

BAERVELDT SHUNT

FDA Adverse Event
Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

CAPSFIX PU SCR.-IN

FDA Adverse Event
Injury ·MPRI·Product code DTB·February 11, 2013

TENDRIL ST

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
Malfunction ·INVAMEX·Product code ILS·July 24, 2014