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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    ULTRACHEM GLUC-DH, ITEM NO. 65048

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ERA® RV 2.5 Partial Offset Female

    FDA UDI
    STERNGOLD DENTAL LLC·00841549101175·ERA Offset female. Attachments are two-part c...

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704260069·

    AURADONICS

    FDA UDI
    AURADONICS INC.·00810033836220·LATEX ELASTICS 1/8" 6.5 oz. - AMBER, 100000 ea....

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0112020·Tap, 4.75 mm

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K0112020·Tap, 4.75mm

    SURGICAL TISSUE MANAGEMENT SYSTEM

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

    MSI BIPOLAR SHEATH

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 9, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    LIFEVEST WCD 3100 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·August 11, 2010

    I-STAT ACT CELITE CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JBP·May 13, 2016