BEUDAMED
    3,037 results · 74ms · 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.

    ACCESS POINT MEDICAL

    FDA Adverse Event
    Other ·ACCESS POINT MEDICAL·Product code ITJ·November 23, 2009

    INTRODUCER, CATHETER (INTRODUCER)

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code DYB·April 2, 2026

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·April 15, 2011

    SOUNDSTAR® ECO DIAGNOSTIC ULTRASOUND CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code OBJ·March 3, 2025

    MIC GASTROSTOMY FEEDING TUBE WITH ENFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·May 7, 2020

    CLAVE

    FDA Adverse Event
    Malfunction ·ICU MEDICAL INC.·Product code FPA·January 6, 2011

    KIT, 14FR INTRODUCER, 13CM&25CM, STERILE

    FDA Adverse Event
    Malfunction ·ABIOMED, INC. - 1220648·Product code DYB·May 15, 2026

    INTRODUCER, CATHETER (INTRODUCER)

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code DYB·May 18, 2026

    UNK_IMPELLA CP

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 5, 2026

    LANTIS COMMANDER 10 USER

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code LNX·June 27, 2006

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 6, 2026

    PREMIUM ONE-STEP

    FDA Adverse Event
    Injury ·INNERDYNE, INC.·Product code GCJ·February 24, 1999

    MIC-KEY GASTRIC-JEJUNAL FEEDING TUBE KIT EXTENSION SETS-16 FR, 1.7CM

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·January 16, 2025

    IMPELLA

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code DYB·April 10, 2026

    IMPELLA

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code OZD·March 5, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 10, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 9, 2026

    UNKNOWN CORTRAK2 TUBE

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·October 15, 2018

    Cordis a Johnson & Johnson Company, RadialSource Spring Wire Transradial Access Kit. Manufacturer Greatbatch Medical 2300 Berkshire Lane North, Minneapolis, MN 55441, Distributor Cordis Corporation 14201 North West 60th Avenue, Miami Lakes, Florida 33014. Baxter's lnfusors SV Elastomeric Infusion Device is a single-use, disposable elastomeric infusion pump indicated tor patients requiring slow, continuous intravenous, intra-arterial, subcutaneous, or epidural administration of medications at a constant flow rate. The device is also indicated for the administration of bolus doses of medication upon patient demand when used in conjunction with the Patient Control Module. lt is suitable for use in the hospital or home setting.

    FDA Enforcement
    Class II ·Terminated·Greatbatch Medical·July 3, 2013

    KIT, 14FR INTRODUCER, 13CM&25CM, STERILE

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code DYB·March 13, 2026