BEUDAMED
    69 results · 21ms · 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 ×

    MODIFIED HYDROPHILIC COATED GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994989802·DRILL 2000011 CANNULATED 7MM

    PIVO 22G

    FDA UDI
    VELANO VASCULAR, INC.·00850984007010·PIVO 22G Compatible device

    SILVERVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948034721·SILVERVENT LINGO-PHON 1 ICF, SIZE 11

    Impression Tray XSM

    FDA UDI
    Access Dental Lab, LLC·00850007728366·Impression Tray Extra Small

    SILVERVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948000108·SILVERVENT 1 IC, SIZE 11

    Avoset Needleless Y-Site without sleeve set

    FDA UDI
    EITAN MEDICAL LTD·17290109152339·

    PediFlex Advanced ILC

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132122471·AO 4.5 MM DRILL

    RECLAIM

    FDA UDI
    DEPUY (IRELAND)·10603295554035·RECLAIM MONOBLOC TRAY INSERT STANDARD DISTAL RE...

    AP213-01-MICROBORE INFUSION SET WITH NON-VENTED SPIKE, SLIDE CLAMP, ADMINISTRATI

    FDA UDI
    EITAN MEDICAL LTD·17290109153183·

    Pin Guide, Left

    FDA UDI
    Treace Medical Concepts, Inc.·00810111221863·Pin Guide, Left

    AspireAssist Skin-Port-US

    FDA UDI
    ASPIRE BARIATRICS, INC.·10857808005549·Skin-Port-US

    Taurus

    FDA UDI
    CTL Medical Corporation·00841732163751·Taurus Implant Case - Base

    AspireAssist A-Tube Kit

    FDA UDI
    ASPIRE BARIATRICS, INC.·10857808005471·AspireAssist A-Tube Kit

    e-vive NMES System with Post-Op Brace; Large/XL, Left

    FDA UDI
    Motive Health, Inc.·00854816006639·e-vive NMES System with Post-Op Brace; Large/XL...

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·BIODIVYSIO AS PS (PHOSPHORYLCHOLINE)COATED STENT DELIVERY SYSTEM

    LIGACLIP MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·LACEY MANUFACTURING CO·Product code GDO·July 28, 2000

    IMMULITE PHENOBARBITAL, MODELS LKPB1, LKPB5

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    WALLGRAFT TRACHEOBRONCHIAL ENDOPROSTHESIS AND UNISTEP DELIVERY SYSTEM

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

    Taurus Pedicle Screw System

    FDA UDI
    SINTX Technologies, Inc.·M555500000011·Taurus Implant Case - Base