BEUDAMED
    22 results · 28ms · 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.

    BARTELS VIRAL RESPIRATORY SCREENING AND IDENTIFICATION KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257024430·OMOMED SHOULDER SUP SILVER RIGHT SIZE IV

    SCANLAN® Needle Holders

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159002973·Jacobson Micro Needle Holder Round Handle

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114162·ROBINS-KRATZ POLISHING CAN, 22GA PK/10

    Creation Willi Geller

    FDA UDI
    KLEMA Dentalprodukte GmbH·ECWG0032041·CC/ Transition Dentine TD-A3,5

    WECK

    FDA UDI
    TELEFLEX INCORPORATED·14026704725332·HORIZON TI ML 24 Clips/Pouch

    WECK

    FDA UDI
    TELEFLEX INCORPORATED·34026704624813·HORIZON TI ML 24 Clips/Pouch

    WECK

    FDA UDI
    TELEFLEX INCORPORATED·24026704696325·HORIZON TI ML 24 Clips/Pouch

    Creation Willi Geller

    FDA UDI
    KLEMA Dentalprodukte GmbH·09010782023624·CC/ Transition Dentine TD-A3,5

    WECK

    FDA UDI
    TELEFLEX INCORPORATED·34026704410270·HORIZON TI ML 24 Clips/Pouch

    WECK

    FDA UDI
    TELEFLEX INCORPORATED·14026704410276·HORIZON TI ML 24 Clips/Pouch

    SCANLAN® Needle Holders

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159019070·Jacobson Micro Needle Holder Round Handle

    WIN-1 TANGO

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PACEMAKER EXTENSION CABLE MODELS 4265,4265A, 4265V, 5265, 5265A, 5265V

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013

    INRATIO

    FDA Adverse Event
    Other ·ALERE SAN DIEGO, INC.·Product code GJS·February 15, 2011

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 22, 2008

    smiths medical PORTEX Tracheal Tube Exchange Guide, 15Ch x 70cm, REF 14-504-68 and REF 14-504-68JP

    FDA Enforcement
    Class II ·Ongoing·Smiths Medical ASD, Inc.·December 4, 2024

    Ace Percutaneous Transluminal Coronary Angioplasty (PTCA) Dilatation Catheter with 1 cm Tip and 20 mm Balloon, Catalog Number H74903628151

    FDA Recall
    Terminated ·Product code LOX·August 20, 2003

    Boston Scientific/Cameron Health SQ-RX Model 1010 subcutaneous pulse generators. The S-ICD System is intended to provide therapy for the treatment of life-threatening ventricular tachyarrhythmias.

    FDA Enforcement
    Class II ·Terminated·Boston Scientific CRM Corp·March 27, 2013