BEUDAMED
    31 results · 20ms · Sources: EU EUDAMED, US FDA

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    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFTSITE (HEFILCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFTSITE (HEFILCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFT SITE (HEFICON A)

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFT SITE (HEFILCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFTSITE (HEFILCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFTSITE (HEFILCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFTSITE (HEFILCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFT SITE (HEFILCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFTSITE (HEFILCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFTSITE (HEFILCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFTSITE (HEFILCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SOFTSITE (HEFILCON A) CONTACT LENS

    Acetabular reamer Ø36 with round tooth

    FDA UDI
    MPS Micro Precision Systems AG·07640187912746·Acetabular reamer for hip arthroplasty

    Sof-Flex

    FDA UDI
    COOK INCORPORATED·00827002177932·Sof-Flex Pediatric Double Pigtail Ureteral Sten...

    3M™ Unitek™ Victory Series™ MBT™

    FDA UDI
    3m do Brasil Ltda.·00652221010735·Victory Series(TM) Bracket MBT(TM) LL3 -6T/3A ....

    Pyxis Pro MedStation

    FDA UDI
    CAREFUSION 303, INC.·10885403529191·Pyxis Pro MedStation Dispensing System cabinet,...

    NOBELREPLACE CC NP 3.5X10MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE USA, LLC·Product code DZE·October 14, 2019

    FDA Pre-Market Approval
    BRYREL SYRUP

    ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC SCIMED INC·Product code DQO·February 15, 2002

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 19, 2017