BEUDAMED
    18 results · 40ms · Sources: EU EUDAMED, US FDA

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    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL·Product code HQL·June 15, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    COLLAMER ULTRAVIOLET ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

    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

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·June 21, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·March 5, 2013

    DEPUY ASR300 ACETABULAR SIZE 56MM

    FDA Adverse Event
    Injury ·DEPUY·Product code KWA·February 9, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 7, 2014

    ACUVUE ABILITI OVERNIGHT THERAPEUTIC LENSES FOR MYOPIA MANAGEMENT

    FDA Adverse Event
    Malfunction ·MENICON CO. LTD.·Product code NUU·January 2, 2024

    COCR HEAD, M, 36/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LPH·March 28, 2023