BEUDAMED
    26 results · 22ms · Sources: EU EUDAMED, US FDA

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    BIOMET CALCANEAL PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526827936·ACHIMED ACHILLES SUPP BLACK V

    MedGyn Aspiration Kit

    FDA UDI
    MEDGYN PRODUCTS, INC.·M803022515·5mm Aspiration Kit

    CarePoint Precision

    FDA UDI
    ALLISON MEDICAL, INC.·00786227225159·25G x 1-1/2" Poly Hub Needle

    Genemed®

    FDA UDI
    SAKURA FINETEK U.S.A., INC.·00615233010117·anti-PD-L1 Rabbit Monoclonal Antibody [RM320], ...

    True Position®

    FDA UDI
    ATLAS SPINE, INC.·M68112080225150·25mm x 15mm Non-Lordotic Spacer

    COATED VICRYL PLUS ANTIBACTERIAL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·April 20, 2006

    COATED VICRYL PLUS ANTIBACTERIAL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·April 20, 2006

    COATED VICRYL PLUS ANTIBACTERIAL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·April 20, 2006

    COATED VICRYL PLUS ANTIBACTERIAL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·April 20, 2006

    BIFURCATED VACCINATING NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDLOGICS ML 4000, MODEL 4000

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    COATED VICRYL PLUS ANTIBACTERIAL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·April 25, 2006

    COATED VICRYL PLUS ANTIBACTERIAL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·April 21, 2006

    CYSTOTOME CYSTOENTEROSTOMY NEEDLE KNIFE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code KNS·March 15, 2019

    CAPIOX HEMOCONCENTRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

    BIOCATH 2 WAY HYDROGEL COATED FOLEY CATHETER, 30CC, 18 FR.

    FDA Adverse Event
    Injury ·BARD SDN. BHD.·Product code EZC·March 20, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·February 15, 2011

    LUMENISONE

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEX·April 1, 2008

    Option-vm Urinary Catheter. Male use only. Latex Free. Sterile, Rx only.

    FDA Enforcement
    Class II ·Terminated·C.R. Bard, Inc.·September 21, 2016