BEUDAMED
    29 results · 30ms · 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 ×

    ULTIMUM EV HEMOSTASIS INTRODUCER (14F), ULTIMUM EV HEMOSTASIS INTRODUCER (16F), ULTIMUM EV HEMOSTASIS INTRODUCER (18F),

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040045091·Vaginal Speculum Pederson Econ

    TruForm

    FDA UDI
    Rmo, Inc.·00885797099815·MX 1-2 BI BD KT N/L UNIV 131

    LINK Endo-Model EVO Knee System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575274734·Replacement set, CoCrMo, UHMWPE, Ti6Al4V, for ...

    ARROW ULTRA 8 INTRA-AORTIC BALLOON CATHETERS (IABS) 8FR 30CC AND 40CC UNIVERSAL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FOCUS

    FDA 510(k)
    FDA Class 2 ·Dental

    IB KIT, BC, W/ CC FT AND JUMPSTART

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MAI·August 14, 2024

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·February 12, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·February 23, 2011

    SERVO VENTILATOR 300A

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·February 7, 2008

    IB KIT, PEEK, NON-COLLAGEN COATED

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MAI·July 16, 2024

    MIS 3.9MM BC ACHILLES SPDBRG W/ KL DX CC

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWC·August 5, 2024

    BIO-COMP INTERFSCRW,FULL THD

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MAI·October 13, 2023

    UNIVERS VAULTLOCK GLENOID TRIAL, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code KWS·June 24, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 23, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 23, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 22, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 22, 2024

    LO-PRO LOCK SCRW TI 4.5X16MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRS·May 3, 2024

    LO-PRO LOCK SCRW TI 4.5X16MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRS·May 3, 2024