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

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    BUN, MODEL BU 104-01

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    1801 P37,GE,2L,1LD,(17&18),144",STKR

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828100687·1801 P37,GE,2L,1LD,(17&18),144",STKR

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES BETTLACH·Product code HWC·June 9, 2015

    11G BLADED MAMMOTOME ST PROBE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code KNW·February 27, 2006

    HD ENDOEYE, MODELS WA50011A, WA50013A, WA50013L, WA50013T, WA50015L

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

    Reprocessed Webster Duo-Decapolar Diagnostic EP Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Active I-PTH Enzyme-Linked Immunosorbent Assay(ELISA), Part Number: DSL-10-8000 The DSL-10-8000 ACTIVE I-PTH Enzyme-Linked Immunosorbent Assay (ELISA) Kit provides materials for the quantitative measurement of I-PTH in serum or plasma. This assay is intended for in vitro diagnostic use as an aid in the diagnosis of hyperparathyroidism

    FDA Recall
    Terminated ·Beckman Coulter Inc.·Product code CEW·March 4, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 6, 2013

    ENTRUST AT

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code LWS·February 15, 2011

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014

    PAEDIATRIC CANNULA, VENOUS

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DWF·June 7, 2023