BEUDAMED
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    AESCULAP, INC.

    FDA registration
    AESCULAP, INC.·318 products·🇺🇸 United States

    AESCULAP, INC.

    FDA registration
    AESCULAP, INC.·4 products·🇺🇸 United States

    AESCULAP, INC., MONOSYN SYNTHETIC ABSORBABLE SURGICAL SUTURE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AESCULAP, INC. SAFIL QUICK SYNTHETIC ABSORBABLE SURGICAL SUTURE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CESPACE BONE CORT CAN 10X16X13.5MM LORDO

    FDA Adverse Event
    Malfunction ·CONTRACT MANUFACTURER: RTI SURGICAL·Product code LMO·May 27, 2016

    AS ENDURO FEMORAL COMPONENT CEMENTED F1R

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·August 31, 2021

    KERRISON BLK COATED 130 UP 180X1MM THIN

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code LRY·January 26, 2016

    KERRISON BLK COATED 130 UP 180X1MM THIN

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code LRY·January 26, 2016

    KERRISON BLK COATED 130 UP 180X1MM THIN

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code LRY·January 26, 2016

    KERRISON BLK COATED 130 UP 180X1MM THIN

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code LRY·January 26, 2016

    MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code HWE·June 7, 2017

    KERRISON BLK COATED 130 UP 180X1MM THIN

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code LRY·January 26, 2016

    CESPACE BONE CORT CAN 9X14X11.5MM LORDO

    FDA Adverse Event
    Malfunction ·CONTRACT MANUFACTURER: RTI SURGICAL·Product code JDN·May 27, 2016

    LIGATURE CLIP 12 MAG.= 144 PCS.

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code FZP·February 4, 2016

    CAIMAN DISP.INSTR.NON ARTICUL.D5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·February 18, 2016

    CAIMAN DISP.INSTR.ARTICULAT.D5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·February 1, 2016

    KERRISON DET130 DEG UP 2MM 180MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code LRY·January 12, 2017

    PROGAV 2.0 VALVE

    FDA Adverse Event
    Malfunction ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·April 30, 2018

    CAIMAN DISP.INSTR.NON ARTICUL.D5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·February 17, 2016

    PROSA VALVE

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·April 30, 2018