BEUDAMED
    122 results · 29ms · Sources: EU EUDAMED, US FDA

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    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILCON(R) (SILAFILCON A) CONTACT LENS DAILY WEAR

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILCON(R) (SILAFILCON A) CONTACT LENS DAILY WEAR

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILCON(R) (SILAFILCON A) CONTACT LENS DAILY WEAR

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILCON(R) (SILAFILCON A) CONTACT LENS DAILY WEAR

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILCON(R) (SILAFILCON A) CONTACT LENS DAILY WEAR

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILCON(R) (SILAFILCON A) CONTACT LENS DAILY WEAR

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILCON(R) (SILAFILCON A) CONTACT LENS DAILY WEAR

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILCON(R) (SILAFILCON A) CONTACT LENS DAILY WEAR

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILCON(R) (SILAFILCON A) CONTACT LENS DAILY WEAR

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILCON(R) (SILAFILCON A) CONTACT LENS DAILY WEAR

    ACCULIF

    FDA UDI
    Stryker Corporation·07613327105858·INSERTION HANDLE ROTATOR KNOB

    BaseVac

    FDA UDI
    R. E. Morrison Equipment Inc·D13028000540·3SUR4.40-1 | 22 User Triple Surgical Vacuum | N...

    SHEFFIELD RING FIXATOR

    FDA UDI
    ORTHOFIX SRL·18053504365860·Spare part, not medical device, not for sale. R...

    0800,APS1,10,N,VL,LT,JW

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828152761·0800,APS1,10,N,VL,LT,JW

    ACUMED

    FDA UDI
    Acumed LLC·10806378039607·Radiolucent VDR Tgt Guide Assy Narrow, R

    SONIALVISION G4

    FDA UDI
    SHIMADZU CORPORATION·04540217064816·

    KODAK EKTACHEM ELECTROLYTE ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·January 28, 1998

    Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold, Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INFUSE BONE GRAFT

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 8, 2014