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

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    PRIMARY CARE SOLUTIONS STERILE SALINE-0.9% SODIUM CHLORIDE FOR DEVICE IRRIGATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Affiniti

    FDA UDI
    TORNIER, INC.·00846832021611·HUMERAL FLAT PLATE CUTTING GUIDE

    PowerPICC SOLO

    FDA UDI
    Bard Access Systems, Inc.·00801741028977·Catheter Placement Kit

    Creation Willi Geller

    FDA UDI
    KLEMA Dentalprodukte GmbH·ECWG0002661·CC/ Effect Enamel SI-02 medium yellow

    NEW METAL STRIPS

    FDA UDI
    Gc America Inc.·14548161391764·NEW METAL STRIPS Refill Package, #1000 Mesh C-W...

    NEW METAL STRIPS

    FDA UDI
    Gc America Inc.·D0470002661·NEW METAL STRIPS Refill Package, #1000 Mesh C-W...

    FlowLogic Agile

    FDA UDI
    SONENDO, INC.·00810209420185·FlowLogic Agile Shaping File 20/.06, 31mm

    SYNTHES (USA) LOCKING CONDYLAR PLATE (LCP) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    FingerClip

    FDA UDI
    Honeywell Healthcare Solutions GmbH·04036616001366·FingerClip F-3412-9 Ohmeda

    LINGUAL BLADED 1X16 20-DEG M S66

    FDA UDI
    AMERICAN TOOTH INDUSTRIES·D772ATI083540002660·

    ASPHERE M SPEC 11/13 36 +3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·September 25, 2013

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·September 25, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·March 12, 2013

    RESTORE PRIME

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 17, 2011

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 14, 2008

    ASPHERE M SPEC 11/13 36 +3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code JDI·June 11, 2012

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·June 11, 2012

    SMR GLENOSPHERE Ø 36MM

    FDA Adverse Event
    Injury ·Product code KWS·June 16, 2021

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 13, 2015