BEUDAMED
    28 results · 21ms · Sources: EU EUDAMED, US FDA

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    JILCO TRACTION-FLEXION CHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092122723·Straumann® TL WN-compatible Ti Base x 4.5mm

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001361·artVeneer life lower anteriors, UIM, C2

    AirLife™

    FDA UDI
    VYAIRE MEDICAL, INC.·10190752116269·AirLife™ Adult Oxygen Mask Vinyl, Under-The-Chi...

    AirLife™

    FDA UDI
    AIRLIFE·10889483570128·AirLife™ Adult Oxygen Mask Vinyl, Under-The-Chi...

    Isolaz

    FDA UDI
    SOLTA MEDICAL·00816995020578·SM IAC ST IV-VI 375

    3M™ Unitek™

    FDA UDI
    3m do Brasil Ltda.·00652221002143·Unitek(TM) Standard Edgewise Bracket Twin U4,5/...

    Elite Expandable Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7401001361·CEI 595 Shaver, 7mm

    Alpha-Omega Services, Inc. Product No: SPECIAL-NFV Description: CUSTOM FLEXIGUIDE NEEDLE, SERIES 15, WITH FEMALE LUER AND STYLET WITH MALE LUER 28CM, SET OF 100 Quantity: 1/PKG Lot No: K00136 L-SPECIAL- NFV. The FlexiGuide is a flexible needle designed to provide an enclosed pathway for localized radiation therapy using a Remote High Dose Rate (HDR) Afterloader or manual Low Dose Rate (LDR) method.

    FDA Recall
    Terminated ·Alpha Omega Services Inc·Product code IWJ·November 15, 2007

    ULTRAPEN REUSABLE PENCIL, MODEL 130350 THROUGH 130353, REUSABLE ACCESSORY ELECTRODE KIT (FOR USE WITH ULTRAPEN PENCIL),

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    K-ASSAY AT-III

    FDA 510(k)
    FDA Class 2 ·Hematology

    2520274-2013-01424

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·March 13, 2013

    CAPSURE SP

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 25, 2011

    ELITE PASS SHUTTLE NEEDLE, BOX OF 5

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIVISION·Product code FMI·February 20, 2008

    Z.S.G.M. CUTTER 3:1 RATIO ( CAUTION: SHARP )

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·February 6, 2023

    MASK OXYGEN MED CONC W/7FT U-CONN-IT TBG

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code BYG·July 23, 2012

    MASK OXYGEN MED CONC W/7FT U-CONN-IT TBG

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code BYG·July 23, 2012

    ZIMMER SKIN GRAFT MESHER

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·February 6, 2023

    UNKNOWN OXFORD TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HRY·March 11, 2020

    LIGHTSHEER EC

    FDA Adverse Event
    Injury ·RH USA, INC.·Product code GEX·August 28, 2012