BEUDAMED
    33 results · 20ms · Sources: EU EUDAMED, US FDA

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    ACUMED SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DeltaForm HD

    FDA UDI
    Merz Dental GmbH·D7091980103·DeltaForm HD lower posteriors, L, C2 -MADE IN G...

    Shur-Clens

    FDA UDI
    Asept Pak, Inc.·00850073677032·Shur-Clens Wound Therapy Solution - 8 oz. bottle.

    CK-MB Test

    FDA UDI
    STANBIO LABORATORY, L.P.·00657498000748·For the Quantitative Determination of Creatine ...

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR79801031·Sprint II Bracket McLaugh/Benn/Trev. .018" max....

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR79801031001·Sprint II Bracket McLaugh/Benn/Trev. .018" max....

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR79801030101·Sprint II Bracket McLaugh/Benn/Trev. .018" max....

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR79801030051·Sprint II Bracket McLaugh/Benn/Trev. .018" max....

    ULTRAZYME PLUS GOT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL.

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Milling Drum Fine

    FDA UDI
    Spierings Orthopaedics B.V.·08720254007892·

    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code JCT·January 15, 2025

    PREMILENE/MONOSYN SET

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL S.A.·Product code GAW·August 7, 2015

    PREMILENE 8/0 (0.4) 60CM 2XDR8 (M)CV

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAW·June 16, 2022

    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 22, 2025

    PREMILENE 6/0 (0.7) 45CM DSMP11 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAW·July 15, 2019

    XMAX MOTOR

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code ERL·February 21, 2013

    ACCU-CHEK ® COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 7, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 5, 2014

    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 1, 2025