BEUDAMED
    121 results · 38ms · 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.

    Graft, Vascular, Synthetic/Biologic Composite

    FDA Pre-Market Approval
    FDA Class 2 ·GELSEAL TM TRIAXIAL VASCULAR GRAFT

    Graft, Vascular, Synthetic/Biologic Composite

    FDA Pre-Market Approval
    FDA Class 2 ·VASCUTEK GELSOFT(TM) VASCULAR GRAFT

    Graft, Vascular, Synthetic/Biologic Composite

    FDA Pre-Market Approval
    FDA Class 2 ·VASCUTEK GELSEAL(TM) VASCULAR GRAFT

    Graft, Vascular, Synthetic/Biologic Composite

    FDA Pre-Market Approval
    FDA Class 2 ·VASCUTEK GELSEAL(TM) VASCULAR GRAFT

    Graft, Vascular, Synthetic/Biologic Composite

    FDA Pre-Market Approval
    FDA Class 2 ·VASCUTEK GELSOFT(TM) VASCULAR GRAFT

    MODEL 6208,6209,6210,6211,6212,6214 (PLI'S)

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ARROW

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 25, 2023

    CODMAN 3000

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 28, 2023

    CODMAN 3000

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 20, 2023

    CODMAN

    FDA Adverse Event
    Death ·CODMAN & SHURTLEFF·Product code LKK·July 18, 2023

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL283 PULSE GENERATOR & MODEL 370/375 SUPPORT S

    Dilator, Cervical, Synthetic, Osmotic, Pregnancy Termination

    FDA Pre-Market Approval
    FDA Class 3 ·DILAPAN-S CERVICAL DILATOR

    ECHELON LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 24, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 28, 2012

    ACCU-CHEK RAPID D LINK INFUSION SET

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code FPA·November 1, 2010

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL283 PULSE GENERATOR & MODEL 370/375 SUPPORT S

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL283 PULSE GENERATOR & MODEL 370/375 SUPPORT S

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AFP PACING SYSTEM

    Programmer, Pacemaker

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 3307, V4.0A PROGRAMMING SOFTWARE AND MODEL 3160 ECG ADAPTER CABLE

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AFP CARDIAC PACING SYSTEM