BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    VIDAS CHLAMYDIA ASSAY VITEK IMMUNDIAG ASSAY SYST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00681490886567·INSTRUMENT 6905787 COMPRESSION FORCEPS

    Sterngold Implant System Guided Crestal Bone Drill 4.3

    FDA UDI
    STERNGOLD DENTAL LLC·00841549118906·Used to countersink site prior to implant place...

    NASAL E.T. TAPE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    AVI MODEL 470CM INFUSION PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SafeClinitubes, Capillary caps (purple), 905-787. The defective capillary caps may be included in capillary tube kits as follows: Clinitubes Kits: 942-890 (D941P-240-85x1), Lot Code: R0048; Clinitubes Kits: 942-892 (D957P-70-100x1), Lot Codes: R0045 through R0050; Clinitubes Kits: 942-893 (D957P-70-125x1), Lot Codes: R0058 through R0063; Clinitubes Kits: 942-898 (D957P-70-70x1), Lot Code: R0019. Each of the kits listed above contains one (1) bag of Capillary Caps, 905-787.

    FDA Recall
    Terminated ·Radiometer America Inc·Product code GIO·June 29, 2006

    INSULIN PUMP PARADIGM 551

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code OZO·June 25, 2014

    MESH - COMPOSIX KUGEL

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·November 17, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013