BEUDAMED
    23 results · 20ms · 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.

    Suture, Nonabsorbable, Silk

    FDA Pre-Market Approval
    FDA Class 2 ·SILK NONABSORBABLE SUTURES, USP

    Suture, Nonabsorbable, Silk

    FDA Pre-Market Approval
    FDA Class 2 ·SILK NONABSORBABLE SUTURES, USP

    Suture, Nonabsorbable, Silk

    FDA Pre-Market Approval
    FDA Class 2 ·SILK NONABSORBABLE SUTURES, USP

    Suture, Nonabsorbable, Silk

    FDA Pre-Market Approval
    FDA Class 2 ·SILK NONABSORBABLE SUTURES, USP

    Suture, Nonabsorbable, Silk

    FDA Pre-Market Approval
    FDA Class 2 ·SILK NONABSORBABLE SUTURES, USP

    Suture, Nonabsorbable, Silk

    FDA Pre-Market Approval
    FDA Class 2 ·SILK NONABSORBABLE SUTURES, USP

    Suture, Nonabsorbable, Silk

    FDA Pre-Market Approval
    FDA Class 2 ·SILK NONABSORBABLE SUTURES, USP

    Suture, Nonabsorbable, Silk

    FDA Pre-Market Approval
    FDA Class 2 ·SILK NONABSORBABLE SUTURES, USP

    Suture, Nonabsorbable, Silk

    FDA Pre-Market Approval
    FDA Class 2 ·SILK NONABSORBABLE SUTURES, USP

    Suture, Nonabsorbable, Silk

    FDA Pre-Market Approval
    FDA Class 2 ·SILK NONABSORBABLE SUTURES, USP

    Suture, Nonabsorbable, Silk

    FDA Pre-Market Approval
    FDA Class 2 ·SILK NONABSORBABLE SUTURES, USP

    W 1

    FDA UDI
    IVOCLAR VIVADENT, INC.·D7075840470·

    Brylic™ / W-98-14-BR-A400-GR

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271130068·

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515029736·Workhorse Post Clamp, coupling, 1"

    DASH Flex 24 Centrifuge, Restek

    FDA UDI
    DRUCKER DIAGNOSTICS·00810052862521·General purpose laboratory centrifuge for sampl...

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·March 28, 2012

    MIDAS REX III MO3

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBB·March 18, 2002

    AUTO SUTURE MULTIFIRE ENDO GIA 30-3.5

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GCJ·June 28, 2000

    FUSA F80B (HF/PS/1.8/H)

    FDA Adverse Event
    Injury ·FRESENIUS·Product code KDI·August 24, 1998

    Intran Plus, Disposable Intrauterine Pressure Catheter System, Part numbers IUP-400, IUP-400S, IUP-450, IUP-450S, IUP-500, IUP-550, IUP-600, IUP-600S, IUP-650, IUP-650S, IUP-700, IUP-750, Sterile, Single Use, Utah Medical Products Inc., 7043 South 300 West, Midvale, Utah 84047.

    FDA Recall
    Terminated ·Utah Medical Products, Inc·Product code HFN·June 16, 2008