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

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    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 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

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·14026704788917·

    LEONE SPA

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

    OsteoMed

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

    DISPOSABLE NEUTRAL ELECTRODE GP202

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

    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·CERAMIC TRANSCEND HIP ARTICULATION

    Chromogenic In Situ Hybridization, Nucleic Acid Amplification, Her2/Neu Gene, Breast Cancer

    FDA Pre-Market Approval
    FDA Class 3 ·INFORM HER2 DUAL ISH DNA PROBE COCKTAIL

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 6, 2018

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS LLC·Product code OYC·July 10, 2019

    Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T12BT

    FDA Enforcement
    Class II ·Ongoing·Covidien, LP·April 10, 2024

    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

    Chromogenic In Situ Hybridization, Nucleic Acid Amplification, Her2/Neu Gene, Breast Cancer

    FDA Pre-Market Approval
    FDA Class 3 ·INFORM HER-2 DUAL ISH DNA PROBE COCKTAIL