BEUDAMED
    27 results · 34ms · Sources: EU EUDAMED, US FDA

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    SOMONA CWG CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA CWG XYYY(X=DIA, YYY=LENGTH-IN MM)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317300041·

    DURAVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948004731·DURAVENT 1 IC, SIZE 12

    Aspida

    FDA UDI
    ALPHATEC SPINE, INC.·00844856062917·12MM LUMBAR PLATE

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694001618·9 Hole Curved Plate

    AngelMed Guardian Programmer Serial Cable, 10 Foot

    FDA UDI
    Avertix Medical Inc.·00850012625094·PROG-003 Serial Cable (10 foot)

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694029995·9 Hole Curved Plate, Sterile

    WhisperPak, M520 V10 H113 T2m, Case 10

    FDA UDI
    Respironics Novametrix, LLC·00884838075566·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694063234·2.0 System 9 Hole Curved Plate Sterile Qty 2

    BIPOLAR COAGULATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ACUCAM CONCEPT IV, MODELS A1222B, A1223B, A1221B, A1121B, A1222C, A10402, A10403, A10401

    FDA 510(k)
    FDA Class 1 ·Dental

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 5/12 MM L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 29, 2023

    HAHN TAPERED IMPLANT Ø5.0 X 8 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·December 11, 2023

    Widex

    FDA UDI
    Widex A/S·05706069605679·Widex UNIQUE U-FP (Silver white ) Telecoil, Vol...

    Widex

    FDA UDI
    Widex A/S·05706069908145·WIDEX MOMENT MRB0 DEMO (Silver Grey ) 110, RIC 10

    Widex

    FDA UDI
    Widex A/S·05706069594768·Widex UNIQUE U-FM BTE (Silver white ) RC coil

    NCB PERIPROSTHETIC FEMUR POLYAXIAL LOCKING PLATE SYSTEM

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HRS·April 4, 2023

    PLAC TEST REAGENT KIT, MODELS 90107, 90112, 90115, 90116, 10-0112, 10-0113, 10-0115

    FDA 510(k)
    FDA Class 2 ·Immunology

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·April 29, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD .·Product code MCM·September 18, 2014