BEUDAMED
    6,553 results · 31ms · 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 ×

    UNK - IMPLANT

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code MIA·February 27, 2026

    Pillow Tilt Small G - MR

    FDA UDI
    IT-V Medizintechnik GmbH·09120074392601·

    UNK - IMPLANT

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code MIA·February 25, 2026

    ASSURE CARDIAC RECOVERY SYSTEM

    FDA Adverse Event
    Malfunction ·KESTRA MEDICAL TECHNOLOGIES, INC.·Product code MVK·October 27, 2022

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·May 6, 2013

    GMRS EXTENSION PIECE 30MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KRO·January 14, 2015

    MRS FEM STEM W/O BODY 11X127MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KRO·June 16, 2014

    GMRS EXTENSION PIECE 80MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KRO·October 23, 2014

    MRS CVD FEM ST W/O BODY 15X127

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KRO·June 23, 2014

    WST 6:1 F. VDW.GOLD/SILVER

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EGS·June 15, 2022

    VDW GOLD/SILVER CONTRA ANGLE

    FDA Adverse Event
    Malfunction ·DENTSPLY VDW GMBH·Product code EGS·October 12, 2021

    WST 6:1 F. VDW.GOLD/SILVER

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EGS·October 26, 2022

    MRH XS/S/M LONG XOVER

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KRO·August 14, 2013

    REVERSE CROSSOVER

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·September 16, 2014

    GMRS DIST FEM COMP STD L 65MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KRO·January 14, 2015

    GMRS Extension Piece, 60 mm; Sterile Stryker Howmedica Osteonics; Howmedica Internation S. de. R.L. Limerick, Ireland. The Global Modular Replacement System is intended to be used with the components of the Howmedica Osteonics Modular Replacement System , the Howmedica Osteonics Modular Rotating Hinge Knee System and/or the Howmedica Osteonics Kinematic Rotating Hinge Knee System in situations where replacement of extensive bone loss in the femur and/or proximal tibia is required. The Proximal Femoral Module and Distal Femoral Module of the GMR may be used together, or with the components of the MRS, in replacement of the total femur.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code KRO·May 5, 2005

    Sera, Reactive And Non-Specific Control, Fta-Abs Test

    FDA classification
    FDA Class 2 ·Sera, Reactive And Non-Specific Control, Fta-Abs Test

    BMR Medical

    FDA registration
    BMR Medical·1 product·🇧🇷 Brazil

    CMR NAVISCAN CORPORATION

    FDA registration
    CMR NAVISCAN CORPORATION·3 products·🇺🇸 United States

    EMR DISTRIBUTORS, INC.

    FDA registration
    EMR DISTRIBUTORS, INC.·3 products·🇺🇸 United States