BEUDAMED
    22 results · 23ms · Sources: EU EUDAMED, US FDA

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    HEMOSIL VON WILLEBRAND ACTIVITY ASSAY

    FDA 510(k)
    FDA Class 2 ·Hematology

    N/A

    FDA UDI
    MEDTRONIC XOMED, INC.·00763000035112·PROSTHESIS 1133005 CUP PISTON .4X4.0 SST

    Robinson

    FDA UDI
    MEDTRONIC XOMED, INC.·00681490034418·PROSTHESIS 1133005 CUP PISTON .4X4.0 SST

    Contours™ Finishing & Polishing Discs Refill Pack 1/2" Medium

    FDA UDI
    DEN-MAT HOLDINGS, LLC·00359883006198·Aluminum oxide dental finishing and polishing a...

    Contours™ Finishing & Polishing Discs Refill Pack 1/2" Medium

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172016704·Aluminum oxide dental finishing and polishing a...

    Primary Lens Set, 28D, 90D, 4 Mirror

    FDA UDI
    KATENA PRODUCTS, INC.·00841668144275·

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0330050·Vise Grip, Large, 5.5mm

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019

    CLYDESDALE PTC SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·October 17, 2019

    MFGD 1318 18 INCH 1 MEGAPIXEL GREYSCALE LCD DISPLAY

    FDA 510(k)
    FDA Class 2 ·Radiology

    DDRVERSA MOTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    MITRACLIP G4 CLIP DELIVERY SYSTEM (MDD)

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code NKM·December 4, 2023

    GOBED+

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 29, 2013

    INFINITI VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·September 29, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·June 17, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·May 27, 2025

    Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium

    FDA Enforcement
    Class II ·Terminated·Exactech, Inc.·November 25, 2020

    VGI MEDICAL VerteLP LATERAL INTERBODY FUSION instrument kit

    FDA Enforcement
    Class II ·Terminated·VGI Medical, LLC·June 13, 2018

    Depuy SIGMA RP TC3 insert; polyethylene tibial insert, Sz 5, 22.5 mm; Ref 96-2366.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005