BEUDAMED
    20 results · 21ms · Sources: EU EUDAMED, US FDA

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    Sculpsure

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

    NA

    FDA UDI
    Richard Wolf GmbH·04055207007372·HYGIENE-FILTER for single use

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704292589·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771048944·K-Wires, Double trocar, .035-inch (.9mm) diamet...

    Key Surgical K-Wires and Steinmann Pins

    FDA UDI
    KEY SURGICAL, INC.·00849771012368·K-Wires, Double trocar, .035-inch (.9mm) diamet...

    K-Wire w. double end trocarpoint 0.90mm/229mm, 6 pcs./unit

    FDA UDI
    mahe medical gmbh·EMAHKM711110·K-Wire w. double end trocarpoint 0.90mm...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659484122·K-Wire w. double end trocarpoint _x000D_...

    ESCHENBACH LOUPE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896019324·ESCHENBACH LOUPE

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383543927·Gutta Percha Points is used to root canal filin...

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072009765·

    HALO ABLATION CATHETER MODEL 90-9100, HALO90 ULTRA ABLATION CATHETER MODEL 90-9200

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

    NON-ABSORBABLE SILK SUTURE

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

    VERTEK II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·November 13, 2025

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 2, 2025

    ISA CO2

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·December 30, 2022

    CONSERVE(R) PLUS SPIKED CUP

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·June 14, 2013

    ABSORBATACK 5MM SINGLE USE ABSORBABLE

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GDW·July 11, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 9.75CM

    FDA Adverse Event
    Injury ·BIOENTERICS CORPORATION·Product code LTI·September 18, 2008

    ASPHERE M SPEC 11/13 36 +0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·November 29, 2012

    ALTRX +4 10D 36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·November 29, 2012