BEUDAMED
    47 results · 25ms · 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 ×

    ELITECH CLINICAL SYSTEMS HBA1C REAGENT, ELITECH CLINCAL SYSTEM HBA1C CALIBRATOR SET, ELITECH CLINICAL

    FDA 510(k)
    FDA Class 2 ·Hematology

    Aira

    FDA UDI
    AIRA, LLC·00810194404054·5.25" X 7.5" - Paper/Blue Film Self-Sealing Ste...

    STAINLESS STEEL BRIGHT ARCHWIRE

    FDA UDI
    Ortho Organizers, Inc.·00190707066642·.016 Lower Stainless Steel Bright Standard Arch...

    HS Stand. Burr, Ø4.0x70, 50k

    FDA UDI
    Bien-Air Surgery SA·07630055506887·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450267356·

    N/A

    FDA UDI
    Doppkon GmbH & Co. KG·04262494463174·Metal Hammer B 56mm, L 200mm

    ATR TECNIKA

    FDA 510(k)
    FDA Class 1 ·Dental

    VERTEX SEALAND L/C ORTHODONTIC SEALANT

    FDA 510(k)
    FDA Class 2 ·Dental

    ADVIA CENTAUR

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code MZP·May 8, 2013

    TERUMO CDI 540 CALIBRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·May 13, 2011

    EPIDURAL CATHETER

    FDA Adverse Event
    Malfunction ·B/BRAUN·Product code BSO·August 4, 2008

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 5, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 13, 2023

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 17, 2024

    LOGIC FEMORAL PS CEM LEFT SZ 3.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·March 5, 2025

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 4, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·June 30, 2022

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 3.5, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 5, 2024

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 1, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 11, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 26, 2023