BEUDAMED
    19 results · 34ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Salivea Dry Mouth Mouthwash, Salivea Dry Mouth Mouthspray

    FDA 510(k)
    FDA Unclassified ·Unknown

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515023505·Volkman Retractor, USA, 2 prongs, sharp, 8 3/4"

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197537179·Titanium Mayo-Hegar Needle Holder 1,8mm ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197537193·Titanium Mayo-Hegar Needle Holder 1,8mm ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197537155·Titanium Mayo-Hegar Needle Holder 1,8mm ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197537162·Titanium Mayo-Hegar Needle Holder 1,8mm ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197537186·Titanium Mayo-Hegar Needle Holder 1,8mm ...

    QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF PDO (POLYDIOXANONE

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

    ENSPIRE DISCECTOMY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD ANGIOCATH IV CATHETER 24GA 0.75IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·November 21, 2019

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

    ARTHREX ANGEL SYSTEM WITH ASPIRATION KIT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code ORG·May 1, 2019

    VERTECEM V+ SYRINGE KIT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code OAR·June 20, 2013

    GREENLIGHT MOXY

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·July 7, 2011

    HOLDING SLEEVE-LONG FOR MATRIX

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·October 17, 2014

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·March 12, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·October 31, 2008