BEUDAMED
    19 results · 20ms · Sources: EU EUDAMED, US FDA

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    ZENITH TRAVELER CHIROPRACTIC TABLE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517302960·Archon Screw, 4.0x22mm S.D. Var Recon

    LinkSymphoKnee

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575253784·Articulating Surfaces, PS+

    LinkSymphoKnee

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575253593·Articulating Surfaces, PS+

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011880222000·dentaform® Snap Band, Tooth 46, Size 22

    LinkSymphoKnee

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575253791·Articulating Surfaces, PS+

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011880222180·dentaform® Snap Band, Tooth 46, Size 22/Roth 18

    LinkSymphoKnee

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575253777·Articulating Surfaces, PS+

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011880222220·dentaform® Snap Band, Tooth 46, Size 22/Roth 22

    LinkSymphoKnee

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575253579·Articulating Surfaces, PS+

    LinkSymphoKnee

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575253807·Articulating Surfaces, PS+

    I.V. START KIT

    FDA 510(k)
    FDA Unclassified ·Unknown

    Reaxon Plus

    FDA 510(k)
    FDA Class 2 ·Neurology

    NA

    FDA UDI
    STRYKER CORPORATION·07613327062977·21 Fr. Cysto Standard Obturator

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 18, 2014

    UNKNOWN TRUFILL PUSHABLE COIL

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code MCG·October 22, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·December 19, 2012

    Male-Female Midsection with the following sizes and model numbers. a. Male-Female Midsection, 40mm, 1 EACH; Model Number: 25001040E b. Male-Female Midsection, 50mm, 1 EACH; Model Number: 25001050E c. Male-Female Midsection, 60mm, 1 EACH; Model Number: 25001060E d. Male-Female Midsection, 70mm, 1 EACH; Model Number: e. Male-Female Midsection, 90mm, 1 EACH; Model Number: 25001090E f. Male-Female Midsection, 110mm, 1 EACH; Model Number: 25001110E g. Male-Female Midsection, 140mm, 1 EACH. Model Number: 25001140E Component of ELEOS SEGMENTAL LIMB SALVAGE SYSTEM

    FDA Enforcement
    Class II ·Ongoing·Onkos Surgical, Inc.·June 4, 2025

    Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026