BEUDAMED
    103 results · 27ms · 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.

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILSOFT (ELASTOFILCON A ) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILSOFT (ELASTOFILCON A ) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILSOFT (ELASTOFILCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILSOFT (ELASTOFILCON A ) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILSOFT (ELASTOFILCON A ) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILSOFT (ELASTOFILCON A ) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·SILSOFT (ELASTOFILCON A ) CONTACT LENS

    O-Ring

    FDA UDI
    Preat Corporation·00842092109106·American Mini Female only

    Preat

    FDA UDI
    Preat Corporation·00842092137925·Sphero Block Abutment Nobel Active/Conical 3.0 ...

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950022434·CALIPER CASTROVIEJO LONG BEAK 45 DEGREE ANGLE 0...

    HEARTLINE RYDER NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896006799·HEARTLINE RYDER NEEDLE HOLDER WITH LOCK TUNGSTE...

    HEARTLINE RYDER NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09928000200·HEARTLINE RYDER NEEDLE HOLDER WITH LOCK TUNGSTE...

    Rampart O

    FDA UDI
    SPINEOLOGY INC.·M7402800020·16x30mm Trial

    NON ADHERANT WOUND BANDAGES

    FDA 510(k)
    FDA Unclassified ·Unknown

    Cardiac Ablation Percutaneous Catheter

    FDA Pre-Market Approval
    FDA Class 3 ·STINGER ABLATION CATHETER; TEMPLINK EXTENSION CABLE

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·GEL-ONE

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·May 8, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 17, 2012

    SYNERGY

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 12, 2010

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·December 22, 2011