BEUDAMED
    64 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    OSSIOfiber™ Compression Screws

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169599512·TRIAL 2193660 O25 IB 27MM 18 DEG 18X60

    COLD PACK, PLASTIC APPLICATOR (MEDICAL GRADE)-NON-CHEMICAL

    FDA 510(k)
    FDA Unclassified ·Unknown

    LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CART 9733856 S7 STAFF ASSEMBLED 110V

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 18, 2019

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 22, 2014

    ARCOM XL RINGLOC ACETABULAR LINER 28MM 10 DEGREE SIZE 24

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·August 5, 2011

    SCRDRIVERSHAFT T25 F/URS

    FDA Adverse Event
    Malfunction ·SYNTHES, USA·Product code HTW·June 27, 2013

    BIOLOX DELTA CER LNR 36MM E

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

    RINGLOC-X E1 H/W 56/36MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·April 27, 2026

    BIOLOX DELTA CER LNR 40MM G

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·April 27, 2026

    CART 9733856 S7 STAFF ASSEMBLED 110V

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 6, 2019

    STEALTHSTATION S7 SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·February 12, 2018

    CART 9734056 S7 STAFF SHRT 100-120V INTL

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 18, 2019

    STEALTHSTATION® S7

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·March 18, 2019

    AVAN E1 INSERT 28 S 52

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·March 6, 2025

    BIOLOX DELTA CER LNR 32MM E

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·September 8, 2025

    RINGLOC BIPOLAR VIVACIT-E

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·September 10, 2025

    CMK OC - RASP S303

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·January 28, 2026

    CMK OC - RASP S303

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·January 28, 2026