BEUDAMED
    56 results · 26ms · 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 ×

    INSTRUMED VESSEL DILATORS, MODEL 65-7XX,65-9XXX,66-1XXX,65-7048-65-7054

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SleepWeaver Elan - Mask & Headgear - Regular - Beige

    FDA UDI
    CIRCADIANCE, LLC·B036100518·SleepWeaver Elan Cloth Nasal PAP Mask & Headgea...

    COOLEY BULLDOG CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921005180·COOLEY BULLDOG CLAMP RING HANDLE STRAIGHT

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319702444·Lister Bandage Scissors 8" (20cm), side angled ...

    Forceps, Dressing, TC, acc. Gerald 18.0cm

    FDA UDI
    Geister Medizintechnik GmbH·04057034020050·Forceps, Dressing, TC, acc. Gerald 18.0cm...

    BONASTENT® Biliary

    FDA UDI
    Sewoon Medical Co., Ltd.·08806369461429·

    Orthoquest

    FDA UDI
    Young Innovations, Inc.·00843471155721·V Nat D 016X022 Lo

    HS Diam. Burr, Ø2.3x70, 50k

    FDA UDI
    Bien-Air Surgery SA·07630055506597·

    Arena-L®

    FDA UDI
    SPINEFRONTIER, INC.·00190361005483·Arena-L, Lordotic 10 degrees, 35X26X18

    Zavation

    FDA UDI
    Zavation LLC·00842166178151·18mm Cervical Drill

    Young Specialties

    FDA UDI
    Young Innovations, Inc.·00840326425268·NiTi SE Archwire, NAT .016x.022 Lower Dimple 10EA

    QUANTA SYSTEM S.P.A.

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM, S.P.A.·Product code GEX·December 21, 2012

    SYNTHES ANTEROLATERAL CALCANEAL PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MACROPRO GEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    CERES

    FDA UDI
    SPINAL ELEMENTS·00840916140090·Ceres® 18mm Cervical Drill

    LCCS

    FDA UDI
    LCCS Products Limited·04895233601713·Single-use RF Cannula

    LCCS

    FDA UDI
    LCCS Products Limited·04895233602611·Single-use RF Cannula

    DREAMSTATION AUTO CPAP

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·January 28, 2025

    ARCOM 28MM RNGLOC LINER HWALL 24

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 8, 2013

    28MM DIA COCR MOD HEAD +9MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·March 8, 2013