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.
    Filters Regulation: Us FDA ×

    DUOPROSS SYRINGES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Bard® Baker Jejunostomy Catheter

    FDA UDI
    C. R. Bard, Inc.·00801741075674·Bard® Baker Jejunostomy Catheter

    Anterior Quad-Tray®

    FDA UDI
    DEN-MAT HOLDINGS, LLC·00359883002800·Dental impression tray, single-use

    Anterior Quad-Tray®

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172000857·Dental impression tray, single-use

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809867794·FOR MEN 20-30 MM HG THIGH MICRO DOT BAND CLOSED...

    3M™ Unitek™ SmartClip™ MBT™

    FDA UDI
    3m do Brasil Ltda.·00652221003430·SmartClip(TM) Self-Ligating Bracket MBT(TM) LR5...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702466874·ELVAREX 3/KNEE HIGH/SLANT-CLOSED TOE/DOTTED 2,5...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702265682·ELVAREX 2/KNEE HIGH/PROFILE-SLANT-OPEN TOE-ELEP...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702445008·Elvarex Forte 3/Knee High/Open Toe/Cocoa

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971574·

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04059993071111·ELVAREX 3/BERMUDA PANTY/WITH SLIP FORM ON BOTH ...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702330304·Elvarex Forte 3/Thigh High/Slant, Closed Toe, E...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702538908·ELVAREX 1/KNEE HIGH/PROFILE-SLANT-OPEN TOE/DOTT...

    DRI-SATE DRY ACID CONCENTRATE FOR BICARBONATE DIALYSATE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    X-POSURE SYSTEM VERSION 2 RAD

    FDA 510(k)
    FDA Class 2 ·Radiology

    ARROW ARTERIAL CATH KIT: 20GA X 5" (12 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQX·June 8, 2017

    9800Q

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 3, 2013

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·April 6, 2011

    FINELINE II

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code DTB·May 8, 2008

    ARROW ARTERIAL CATH KIT: 20GA X 5" (12 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQX·June 8, 2017