BEUDAMED
    24 results · 22ms · Sources: EU EUDAMED, US FDA

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    Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SpheRx

    FDA UDI
    Nuvasive, Inc.·00887517442277·SpheRx II Tap, 6.5mm

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776182137·Brun Curette he hdl str oval

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361023449·Ø10MM SLOTTED FUSION SCREW, GEN II, SACROFUSE, ...

    Ballard* Multi-Access Port Replacement Catheter

    FDA UDI
    Avanos Medical, Inc.·00609038101132·BALLARD* Multi-Access Port Catheter, Replacement

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780383475·Integra® Jarit® Bruns Oval Cup Curette, 9-1/4",...

    MC2 TWO-STAGE VENOUS CANNULA, OVAL MC2 TWO-STAGE VENOUS CANNULA, THIN WALL TWO-STAGE VENOUS CANNULA, MC2X THREE-STAGE VE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REFLEXION CANNULATOR STEERABLE ELECTROPHYSIOLOGY CATHETER WITH LUMEN, MODEL 402805

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 28, 2025

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FRN·November 24, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·July 18, 2013

    KimVent* Multi-Access Port Replacement Catheter for Adults, Endotracheal,16 F (Product Code 240165-5) A tracheobronchial suction catheter is a device that is attached to a port of the airway circuit for use as needed to aspirate liquids or semisolids from a patient's upper airway.

    FDA Enforcement
    Class II ·Terminated·Halyard Health, Inc·September 9, 2015

    WISE CRT SYSTEM

    FDA Adverse Event
    Injury ·EBR SYSTEMS, INC·Product code SEG·September 5, 2025

    LCP DRILL SLEEVE 5 F/DRILL BITS Ø4.3

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·June 9, 2023

    EHTHYLENE OXIDE STERILANT IN MEDISYSTEMS A/V BLOODLINES

    FDA Adverse Event
    Injury ·MEDISYSTEMS·Product code FJK·June 9, 1999

    MEDISYSTEMS HEMODIALYSIS BLOOD TUBING SET

    FDA Adverse Event
    Other ·MEDISYSTEMS·Product code FJK·June 18, 1999

    KimVent* Multi-Access Port Replacement Catheter for Adults, Endotracheal,16 F (Product Code 240165-5) A tracheobronchial suction catheter is a device that is attached to a port of the airway circuit for use as needed to aspirate liquids or semisolids from a patient's upper airway.

    FDA Recall
    Terminated ·Halyard Health, Inc·Product code BSY·July 29, 2015

    KIMVENT MULTI-PORT, DSY, ENDO, REP CATH 16FR, ALT CODE 240165

    FDA Adverse Event
    Injury ·HALYARD HEALTH·Product code BSY·February 3, 2017

    KIMVENT MULTI-PORT, DSY, ENDO, REP CATH 16FR, ALT CODE 240165

    FDA Adverse Event
    Malfunction ·HALYARD HEALTH·Product code BSY·March 1, 2016