BEUDAMED
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    APEX KNEE MODULAR TIBIA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964072925·Endo Carry-On Procedure Kit

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00850038691042·

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·July 13, 2004

    ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101

    FDA 510(k)
    FDA Unclassified ·Unknown

    EEI SLUSH PAN DRAPE

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

    HYER SCHULTE BREAST IMPLANTS

    FDA Adverse Event
    Injury ·HEYER SCHULTE CORP, SUBSIDARY·Product code FTR·July 21, 1994

    UNK

    FDA Adverse Event
    Injury ·SMITH & NEPHEW PERRY·Product code LYY·October 19, 1998

    CM DRIVE ACQUA IMPLANT 4.3X16

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 22, 2019

    SILTEX SALINE MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FWM·May 18, 1998

    SILTEX LOW BLEED GEL-FILLED MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·MENTOR·Product code FTR·May 14, 1998

    UNK

    FDA Adverse Event
    Other ·SAFESKIN CORP.·Product code LYY·February 19, 1999

    ZIMMER AIR DERMATOME

    FDA Adverse Event
    Injury ·ZIMMER - PATIENT CARE·Product code GFD·May 20, 1994

    CM DRIVE ACQUA IMPLANT 3.5X11.5

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 13, 2019

    GM DRIVE ACQUA IMPLANT 4.3X13

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 26, 2019

    GM DRIVE ACQUA IMPLANT 4.3X11.5

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 26, 2019

    ACCUFIX

    FDA Adverse Event
    Injury ·TELECTRONICS PACING SYSTEMS·Product code DTB·April 14, 1999

    CM ALVIM IMPLANT 3.5X13

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 8, 2019

    VENA TECH

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL, INC.·Product code DTK·April 15, 1999

    STARR-EDWARDS

    FDA Adverse Event
    Death ·STARR EDWARDS·July 29, 1994