BEUDAMED
    26 results · 33ms · Sources: EU EUDAMED, US FDA

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    Nitrile Patient Examination Gloves Blue Tested For Use With Chemotherapy Drugs, Nitrile Patient Examination Gloves Blue Violet Tested For Use With Chemotherapy Drugs,Nitrile Patient Examination Gloves Black Tested For Use With Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517189127·MaXcess Access Blade, 40mm Center

    Needle aspiration and injection

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113646·RETROBULBAR NEEDLE 23GA 38MM

    16PW - Heat Stress Relief

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588130408·Heat Stress Relief - 16 Poly White

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0130400·ROD REDUCER, AXIAL

    CERAMIR CROWN & BRIDGE

    FDA 510(k)
    FDA Class 2 ·Dental

    LIGHT SABER INTRODUCER NEEDLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    UNKNOWN NEXEL ULNAR ARTICULATION KIT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·January 7, 2019

    COMPR SRS MOD STEM - 12X100MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWT·January 7, 2019

    UNKNOWN NEXEL ULNAR COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·January 7, 2019

    COMPR SRS IC SEG - 60MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWT·January 7, 2019

    ALLEGRETTO WAVE-EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·October 24, 2014

    LINOX SD 60/16

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code LWS·August 9, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 9, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code JPA·September 17, 2009

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·November 4, 2009

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code JPA·October 30, 2009

    INRATIO2

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·July 6, 2009

    NEXEL ULNAR COMPONENT PLASMA SPRAYED SIZE 5 115 MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·December 17, 2018

    NEXEL ARTICULATION KIT SIZE 5/6

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·December 17, 2018