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

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    OMEGA LABORATORIES HAIR DRUG SCREENING ASSAY FOR COCAINE AND COCAINE METABOLITES

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517597205·CoRoent Large MP Ti, 11x9x28mm 12°

    LINK Instruments - Trial implants and size gauges

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575036486·Hip prosthesis socket pusher - Screw-In Acetabu...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587P13112870·13mm PLIF Implant 11mm Wide 28mm Length, 7 deg ...

    BIOFRIEND BIOMASK SURGICAL FACEMASK, MODELS UNIVERSAL BF-200-2001 AND PREMIUM BF-200-3013

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

    B-SMART, MODEL B-01

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021

    IMRI REGISTRATION MATRIX FOR GE HEADHOLDER

    FDA Adverse Event
    Other ·BRAINLAB AG·Product code HAW·May 22, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 16, 2011

    LCS COMP RP INSERT LG 10MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code NJL·August 20, 2008

    Single Shot Epidural Tray - 18G Catalog Number: 8139R2

    FDA Enforcement
    Class II ·Terminated·Busse Hospital Disposables, Inc.·June 8, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·October 15, 2021