BEUDAMED
    148 results · 24ms · Sources: EU EUDAMED, US FDA

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    CELL RECOVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Corin TriFit CF Hip Stem

    FDA UDI
    CORIN LTD·05055343898291·TriFit™ CF Stem Standard Size 4

    SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295231967·SIGMA FEMORAL CRUCIATE RETAINING CEMENTED 4 LEFT

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR89600041·Mand. 2. Molar band W-Fit left 04

    Eye Shield

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111123·FOX EYE SHIELD ALUMINUM

    Nx Nail Instrument Kit

    FDA UDI
    Eca Medical Instruments·00857676008393·3.5mm NX Nail

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR89600040501·Mand. 2. Molar band W-Fit left 04

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR89600040101·Mand. 2. Molar band W-Fit left 04

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR89600040051·Mand. 2. Molar band W-Fit left 04

    Crosstella OTW

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CALDERA MESH

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

    SIGMA PLI GVF INS 4 8MM

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code JWH·December 18, 2017

    PFC SIGMA MOD TIB TRAY CEM SZ4

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code JWH·December 18, 2017

    PFC*SIGMA C/R NPOR FEM LT SZ 4

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code LXH·December 18, 2017

    Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes

    FDA Pre-Market Approval
    FDA Class 3 ·THINLINE ENDOCARDIAL PACING LEADS

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    JUMAO MEDICAL EQUIPMENT·Product code IOR·February 13, 2013

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code CGA·January 13, 2011

    8CM ANGLE ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 13, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 24, 2019

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 11, 2022