BEUDAMED
    22 results · 26ms · Sources: EU EUDAMED, US FDA

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    TRIGLYCERIDE REAGENT (COLOR)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Alice

    FDA UDI
    Rmo, Inc.·00885797488824·ROTH ALICE 3-3 018 MAX HK3 6 BKTS

    NTI

    FDA UDI
    NTI - Kahla GmbH Rotary Dental Instruments·E310801012MFG1·NTI Diamond Medium FG

    NTI

    FDA UDI
    NTI - Kahla GmbH Rotary Dental Instruments·E310801012CFG1·NTI Diamond Coarse FG

    NTI

    FDA UDI
    NTI - Kahla GmbH Rotary Dental Instruments·E310801012FFG1·NTI Diamond Fine FG

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930780101230·10" Bayonet Bipolar Fcp 1.0mm Cvd Down

    Electroplated diamond RA 801 012

    FDA UDI
    Diaswiss SA·07630049960237·Dental diamond instrument for intraoral use

    V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIGITAL INTEGRATION SYSTEM, DIS2000

    FDA 510(k)
    FDA Class 2 ·Radiology

    BUSCH®, BNA®

    FDA UDI
    BUSCH & CO. GmbH & Co. KG·D8120340211·Diamond, round, coarse grit, green ring

    MAXCUT DIAMOND BURS (6/pk) FINE 8801-012

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D7781008801121·MAXCUT DIAMOND BURS (6/pk) Shape: Round; Size (...

    MAXCUT DIAMOND BURS (6/pk) CRS 6801-012

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D7781006801121·MAXCUT DIAMOND BURS (6/pk) Shape: Round; Size (...

    MAXCUT DIAMOND BURS (6/pk) MED 801-012

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D778100801121·MAXCUT DIAMOND BURS (6/pk) Shape: Round; Size (...

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code KXA·May 8, 2014

    ULTHERA

    FDA Adverse Event
    Injury ·.·Product code GEI·October 18, 2012

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·September 21, 2007

    ELEKTA UNITY

    FDA Adverse Event
    Malfunction ·ELEKTA SOLUTIONS AB·Product code IYE·September 12, 2025

    ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use within the nasal and nasopharyngeal lumen.

    FDA Enforcement
    Class II ·Terminated·Olympus Corporation of the Americas·June 17, 2020

    ELEKTA UNITY

    FDA Adverse Event
    Malfunction ·ELEKTA SOLUTIONS AB·Product code IYE·June 4, 2025

    DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)

    FDA Enforcement
    Class II ·Ongoing·Pro-Med Instruments Gmbh·June 4, 2025