BEUDAMED
    217 results · 28ms · Sources: EU EUDAMED, US FDA

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    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·W-55 (METHAFILCON A) AND HORIZON 55 SOFT EXTENDED WEAR CONTACT LENSES

    ICU Medical

    FDA UDI
    ICU MEDICAL, INC.·00887709018235·100" (254 cm) Appx 12.4 mL, 15 Drop 24 Hour Adm...

    247

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935105657·

    Transurethral Occlusion Insert, Urinary Incontinence-Control, Female

    FDA Pre-Market Approval
    FDA Class 3 ·FEMSOFT URETHRAL INSERT

    BALLOON URETERAL DILATORS, ACCENT DG BALLOON URETERAL DILATOR SET, ASCEND BALLOON DILATION CATHETERS, BALLOON DILATION C

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Transurethral Occlusion Insert, Urinary Incontinence-Control, Female

    FDA Pre-Market Approval
    FDA Class 3 ·FEMSOFT URETHRAL INSERT

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·ALBERTA LENS S (SULFOCON A) RGP CONTACT LENS

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·ALBERTA LENS S (SULFOCON A) RGP CONTACT LENS

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·ALBERTA LENS S (SULFOCON A) RGP CONTACT LENS

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·ALBERTA LENS S (SULFOCON A) RGP CONTACT LENS

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·ALBERTA LENS S (SULFOCON A) RGP CONTACT LENS

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·ALBERTA LENS S (SULFOCON A) RGP CONTACT LENS

    Transurethral Occlusion Insert, Urinary Incontinence-Control, Female

    FDA Pre-Market Approval
    FDA Class 3 ·FEMSOFT URETHRAL INSERT

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·ALBERTA LENS S (SULFOCON A) RGP CONTACT LENS

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·ALBERTA LENS S (SULFOCON A) RGP CONTACT LENS

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·ALBERTA LENS S (SULFOCON A) RGP CONTACT LENS

    SIMILAR DEVICE S7001, PMA # P990071

    FDA Adverse Event
    Malfunction ·STOCKERT GMBH·Product code LPB·November 13, 2014

    SIMILAR DEVICE S7001, PMA # P990071

    FDA Adverse Event
    Malfunction ·STOCKERT GMBH·Product code LPB·March 10, 2016

    SIMILAR DEVICE S7001, PMA # P990071

    FDA Adverse Event
    Malfunction ·STOCKERT GMBH·Product code LPB·August 31, 2017

    SIMILAR DEVICE S7001, PMA # P990071

    FDA Adverse Event
    Malfunction ·STOCKERT GMBH·Product code LPB·May 19, 2016