BEUDAMED
    24 results · 33ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Triton Canister System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814527·GENUMEDI SAND SIZE I

    CASTROVIEJO FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896073555·CASTROVIEJO FORCEPS WITH TYING PLATFORM FENESTR...

    AYERS ROCK CERVICAL CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PHTIP DISPOSABLE ISFET CATHETER

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

    LEAD EXTRACTION EVOLUTION MECHANICAL DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DRE·October 22, 2018

    LEAD EXTRACTION EVOLUTION MECHANICAL DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VANDERGRIFT INC·Product code DRE·October 22, 2018

    LEAD EXTRACTION STEADYSHEATH¿ EVOLUTION® TISSUE STABILIZATION SHEATH

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DRE·June 12, 2017

    LEAD EXTRACTION STEADYSHEATH¿ EVOLUTION® TISSUE STABILIZATION SHEATH

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DRE·January 10, 2018

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 6, 2025

    LEAD EXTRACTION EVOLUTION MECHANICAL DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DRE·October 16, 2018

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·June 3, 2013

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 30, 2014

    SIDNE SMART 40L CORE INSUFFLATOR

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code HIF·June 20, 2011

    LEAD EXTRACTION EVOLUTION MECHANICAL DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VASCULAR INC.·Product code DRE·December 7, 2018

    Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium

    FDA Enforcement
    Class II ·Terminated·Exactech, Inc.·November 25, 2020

    LEAD EXTRACTION EVOLUTION MECHANICAL DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DRE·October 15, 2018

    LEAD EXTRACTION EVOLUTION MECHANICAL DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DRE·April 13, 2017

    LEAD EXTRACTION EVOLUTION MECHANICAL DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VANDERGRIFT INC·Product code DRE·December 11, 2019

    LEAD EXTRACTION EVOLUTION SHORTIE MECHANICAL DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DRE·March 22, 2017