BEUDAMED
    47 results · 12ms · Sources: EU EUDAMED, US FDA

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    Product Desc: Product Name: A-OK SATINCRESCENT FULL HANDLE2.3MM ANG Model/Catalog Number: 8065990002 Software Version: N/A Product Description: Ophthalmic knife Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HNN·July 15, 2024

    Product Desc: Product Name: A-OK SATINSLIT FULL HANDLE2.75MM ANG SG Model/Catalog Number: 8065992761 Software Version: N/A Product Description: Ophthalmic knife Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HNN·July 15, 2024

    Product Desc: Product Name: A-OK 19G V-LANCE FULL HANDLE1.6MM SATIN Model/Catalog Number: 8065911901 Software Version: N/A Product Description: Ophthalmic knife Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HNN·July 15, 2024

    ClubMax Laser Projection Series

    FDA Recall
    Open, Classified ·Gk Photonics Inc·Product code REA·July 10, 2019

    Logolas Laser Projection Series

    FDA Recall
    Open, Classified ·Gk Photonics Inc·Product code REA·July 10, 2019

    Burstberry Laser Projection Series

    FDA Recall
    Open, Classified ·Gk Photonics Inc·Product code REA·July 10, 2019

    Atom Laser Projection Series

    FDA Recall
    Open, Classified ·Gk Photonics Inc·Product code REA·July 10, 2019

    Spectrum Laser Projection Series

    FDA Recall
    Open, Classified ·Gk Photonics Inc·Product code BRX·July 10, 2019

    Maxim Laser Projection Series

    FDA Recall
    Open, Classified ·Gk Photonics Inc·Product code REA·July 10, 2019

    20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version: N/A Product Description: Ophthalmic knife Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HNN·April 22, 2024

    ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065921541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HNN·April 22, 2024

    ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HNN·April 22, 2024

    ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HNN·April 22, 2024

    BECKMAN COULTER, INC. a. COULTER DxH Diff Pack REAGENT, DIFF PK FP DXHCOULTR, Catalog #628020. b. COULTER DxH Cleaner REAGENT, CLEANER FP DXH 10LCOULTR Catalog #628023. c. DxH 500 Series Lyse LYSE, VERSA SOL DXH 500 SERIES(0.5L/KT) Catalog # B36846. d. DxH 500 Series Cleaner CLEANER, COULTER CLENZ DXH 500SERIES (0.5L/KT) Catalog # B36868

    FDA Recall
    Open, Classified ·Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233·Product code GGK·May 25, 2022

    Product Desc: Product Name: CLEARCUT SAFETY INTREPID SB,2.4 Model/Catalog Number: 8065772445 Software Version: N/A Product Description: Ophthalmic knife Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HNN·July 15, 2024

    Product Desc: Product Name: CLEARCUT HP2 DB SLIT 3.2MM ANGCE Model/Catalog Number: 8065983265 Software Version: N/A Product Description: Ophthalmic knife Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HNN·July 15, 2024

    Product Name: TOTALPLUS,25+ 7.5CPM VALV WD6 Model/Catalog Number: 8065751618 Software Version: N/A Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HQC·July 15, 2024

    Product Name: 25+ CMB PAK 10K CPM,V,STD 0.9 Model/Catalog Number: 8065752450 Software Version: N/A Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HQC·July 15, 2024

    Product Name: TOTAL PLUS,25+,10K VALVE WD Model/Catalog Number: 8065752438 Software Version: N/A Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HQC·July 15, 2024

    Product Name: 25GA VALVED ENTRY SYSTEM,3CT Model/Catalog Number: 8065751658 Software Version: N/A Product Description: Valved Trocar Entry System Component: N/A

    FDA Recall
    Open, Classified ·Alcon Research LLC Aspex Facility·Product code HQC·July 15, 2024