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

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    STRATAFIX UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·January 30, 2026

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·January 30, 2026

    MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAN·January 30, 2026

    TEOSYAL RHA 4

    FDA Adverse Event
    Injury ·TEOXANE SA·Product code LMH·April 17, 2019

    TEOSYAL RHA 4

    FDA Adverse Event
    Injury ·TEOXANE SA·Product code LMH·July 23, 2019

    TEOSYAL RHA 3

    FDA Adverse Event
    Injury ·TEOXANE SA·Product code LMH·November 8, 2019

    TEOSYAL RHA 3

    FDA Adverse Event
    Injury ·TEOXANE SA·Product code LMH·February 4, 2020

    TEOSYAL RHA 2

    FDA Adverse Event
    Injury ·TEOXANE SA·Product code LMH·July 23, 2019

    TEOSYAL RHA 3

    FDA Adverse Event
    Injury ·TEOXANE SA·Product code LMH·July 23, 2019

    ALLERGAN COOLSCULPTING

    FDA Adverse Event
    Injury ·ALLERGAN / ZELTIQ AESTHETICS INC.·Product code OOK·April 29, 2020

    FACE PACK AESTHETIC SURGERY AESTHETIC SURGERY CONTENTS: (15) APPLICATOR COTION 6" WOOD (60) GAUZE SPONGE 4" X 4" 16 PLY SOFT LIF (2) NEEDLE SPINAL ANEST 22G X 3 Y2 LIF (8) TOWELS CLOTH HUCK BLUE LIF (2) SYRINGE 10CC WITHOUT NEEDLE LUER LOCK LIF (6) BLADE #15 CARBON RIB (1) SHEET ENT SPLIT 110" X 77" SMS L/F (3) *Pr. GLOVE PERRY SURG # 7.5 LATEX (5) SPONGE LAP PREWASH 18" X 18" XRD LIF (1) COVER TABLE REINFORCED 50" X 90" LIF (2) COTTON BALL MED (3) *Pr. GLOVE PERRY SURG # 7 LATEX (1) DRAPE INST. MAGNETIC 10" X 16" L/F (2) NEEDLE 30G X 1 DISP LIF (1) MARKER SKIN WITH RULER LIF (4) LABELS FOR SKIN MARKERS 1.25 X Y2 (1) COUNTER NEEDLE AND BLADE 15C FOAM I MAG STRIP LIF (2) GOWN SOFT SMS STD X-LGE SET IN SLEEVE LIF (1) RULER 6" FLEXIBLE (1) BAG ZIP LOCK 6" X 10" PLASTIC Product Usage: EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.

    FDA Enforcement
    Class I ·Terminated·Customed, Inc·September 10, 2014

    TEOXANE SA

    FDA Adverse Event
    Injury ·TEOXANE SA·Product code LMH·February 4, 2020

    REV-LITE Q SWITCHED LASER

    FDA Adverse Event
    Injury ·CYNOSURE, INC·Product code GEX·April 12, 2017

    STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·January 25, 2019

    IDRT, UNKNOWN

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code MDD·August 8, 2019

    GALAFLEX

    FDA Adverse Event
    Injury ·TEPHA, INC. - 3005670760·Product code OOD·April 16, 2026

    MERZ AESTHETICS, 27G X 1.0 " (25MM) Cannula, Sterile R, QTY 20, Model 9015M1X20, Distributed by Merz Aesthetics, In., Manufactured by TSK Laboratory. The intended use of the Cannula is the injection of fluids into, or withdrawal of fluids from, parts of the body below the surface of the skin.

    FDA Recall
    Terminated ·Merz Aesthetics, Inc.·Product code FMI·December 16, 2011

    TEOSYAL RHA 3

    FDA Adverse Event
    Injury ·TEOXANE SA·Product code LMH·January 23, 2019

    TEOSYAL RHA 2

    FDA Adverse Event
    Injury ·TEOXANE SA·Product code LMH·March 28, 2019

    BELOTERO BALANCE

    FDA Adverse Event
    Injury ·ANTEIS S.A.·Product code LMH·January 17, 2021