BEUDAMED
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    FDA UDI
    EASTERN BUSINESS FORMS INC·00860802000345·903 Filter Paper

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    FDA UDI
    EASTERN BUSINESS FORMS INC·00850039198038·LFP Alpha-Spot Kit

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    EASTERN BUSINESS FORMS INC·00860802000383·903 Filter Paper

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    FDA UDI
    EASTERN BUSINESS FORMS INC·00850039198021·

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    EASTERN BUSINESS FORMS INC·00850039198007·903 Filter Paper

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    EASTERN BUSINESS FORMS INC·00860802000321·903 Filter Paper

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    EASTERN BUSINESS FORMS INC·00850039198045·

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    FDA UDI
    EASTERN BUSINESS FORMS INC·00860802000390·LFP Alpha-Spot Kit

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    FDA UDI
    EASTERN BUSINESS FORMS INC·00850039198014·903 Filter Paper Lot#-variable

    bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a component-non-sterile sample for evaluation purposes REF# BVI 58000587

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code OJK·October 8, 2021

    bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a component REF# 58000572 REF#: 373809

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code OJK·October 8, 2021

    Beaver Xstar Crescent Knife, 2.5mm, 55 degrees, bevel down. Intended for or cataract surgery. REF#: 373809

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code HNN·October 8, 2021

    bvi CustomEyes Kit-AMO Germany GmbH Katarakt-set - Dr. Wagner: CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a component a) REF# 588221 REF#: 373809

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code OJK·October 8, 2021

    Advance 35LP Low-Profile PTA Balloon Dilatation Catheter; Catalog numbers: PTA5-35-135-6-2 .0 and PTA5-35-135-4-4 .0; UDI: 10827002522647 and 10827002522524 Product Usage: The Advance 35LP Low Profile PTA Balloon Dilation Catheter is indicated for percutaneous transluminal angioplasty (PTA) of lesions in peripheral arteries including iliac, renal, popliteal, infrapopliteal, femoral and iliofemoral as well as obstructive lesions of native or synthetic arteriovenous dialysis fistulae.

    FDA Recall
    Terminated ·Cook Inc.·Product code DQY·April 16, 2018

    Malosa Core LASIK Pack 2-Medical Refractive Kit- intended to be used to aid in cataract, corneal, or refractive surgery. Part Number: MMK100/2

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code PZG·November 17, 2021

    Malosa Core Phaco Pack 2- Medical Refractive Kit intended to be used to aid in cataract, corneal, or refractive surgery. Part Number: MMK834/1

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code PZG·November 17, 2021

    Malosa Core SMILE Pack 2-Beaver-Visitec- A Medical Refractive Kit intended to be used to aid in cataract, corneal, or refractive surgery. Part Number: MMK967

    FDA Recall
    Open, Classified ·Beaver Visitec International, Inc.·Product code PZG·November 17, 2021