BEUDAMED
    22 results · 24ms · Sources: EU EUDAMED, US FDA

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    DISPOSABLE NEUTRAL ELECTRODE GP202

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

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707010005·CALIBRA 1ST MOLAR BANDS n.UL 27

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694025652·Left L Plate, 12mm

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA Pre-Market Approval
    FDA Class 2 ·ARTUS CMV RGQ MDX KIT

    ELECTROTORQUE TLC

    FDA 510(k)
    FDA Class 1 ·Dental

    GELFLEX SYNERGY SOFT LENS HIOXFILCON 49% WATER CONTENT CLEAR OR BLUE VISITINT; GELFLEX HIOXIFILCON SOFT CONTACT LENS 49%

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA Pre-Market Approval
    FDA Class 2 ·Artus CMV RGQ and QS-RGQ MDx Kit

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA Pre-Market Approval
    FDA Class 2 ·artus CMV RGQ MDx Kit and artus CMV QS_RGQ MDx Kit

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA Pre-Market Approval
    FDA Class 2 ·ARTUS CMV RGQ MDX KIT

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA Pre-Market Approval
    FDA Class 2 ·ARTUS CMV RGQ MDX KIT

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA Pre-Market Approval
    FDA Class 2 ·artus CMV RGQ MDx Kit and artus CMV QS-RGO MDx Kit

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA Pre-Market Approval
    FDA Class 2 ·artus CMV RGQ MDx Kit and artus CMV QS-RGQ MDx Kit

    DORMA 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 16, 2022

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 24, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FSA·September 30, 2014

    PROVISC

    FDA Adverse Event
    Injury ·ALCON - BELGIUM/S.A. ALCON-COUVREUR N.V.·Product code LZP·June 10, 2011

    BD VACUTAINER® SERUM PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·May 14, 2025

    BD VACUTAINER® SERUM PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·May 14, 2025

    BD VACUTAINER® SERUM PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·May 14, 2025

    BD VACUTAINER® SERUM PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·May 14, 2025