BEUDAMED
    49 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 ×

    HARDYDISK CEFAMANDOLE, 30MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994989703·CALIPER 2000022

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950023578·RONGEUR CLEVELAND 4A 6-3/4" 17CM

    SABLE Rotamax PRO KL

    FDA UDI
    Sable Industries Inc·00841359010049·Sable RotaMax Pro KL Interchangeable Fiber Opti...

    Dermagold100

    FDA UDI
    MTS Medical AG·04260484571823·The OW100S is indicated to provide acoustic pre...

    LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022

    FDA Recall
    Open, Classified ·Physio-Control, Inc.·Product code MKJ·September 29, 2023

    LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022

    FDA Enforcement
    Class II ·Ongoing·Physio-Control, Inc.·November 22, 2023

    AP417-01- MICROBORE YELLOW MARKED INFUSION SET WITH NON-VENTED SPIKE AND NEURAXI

    FDA UDI
    EITAN MEDICAL LTD·17290109153206·

    AP206-01- INFUSION SET WITH NON-VENTED SPIKE, FX ADMINISTRATION CASSETTE

    FDA UDI
    EITAN MEDICAL LTD·17290109154623·

    AP416-01 MICROBORE WITH 2 FEMALE LUER LOCKS AND A BACK CHECK VALVE

    FDA UDI
    EITAN MEDICAL LTD·17290109150465·

    General Instrument

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132124918·Rod Cutter

    Pin Guide, Right

    FDA UDI
    Treace Medical Concepts, Inc.·00810111221979·Pin Guide, Right

    AP417-01 MICROBORE EPIDURAL YELLOW MARKED ADMINISTRATION SET WITH VE

    FDA UDI
    EITAN MEDICAL LTD·17290109154920·MICROBORE EPIDURAL YELLOW MARKED ADMINI...

    AP206-01 INFUSION SET WITH NON-VENTED SPIKE, 1.2 FILTER AND NEEDELESS Y-SITE

    FDA UDI
    EITAN MEDICAL LTD·17290109159284·

    AP417-01

    FDA UDI
    EITAN MEDICAL LTD·17290109154807·

    SONIALVISON G4

    FDA UDI
    SHIMADZU CORPORATION·04540217041213·

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·BESTENT 2 OVER-THE-WIRE (OTW)/RAPID EXCHANGE CORONARY STENT DELIVERY SYSTEM

    Panama™

    FDA UDI
    FLOSPINE LLC·B1830810000220·1-Level, 22mm Cervical Plate

    MAGNA 5000 PHASED ARRAY CTL SPINE COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    IMMULITE PHENOBARBITAL, MODELS LKPB1, LKPB5

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology