BEUDAMED
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    CRESOLPHTHALEIN COMPLEXONE, CALCIUM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NA

    FDA UDI
    Richard Wolf GmbH·04055207044599·ALIGNMENT WIRE GUIDE STANDARD SZ 2.5 for tibia...

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556704841·GC Initial™ Ti Shoulder Transpa ST-31, 20g

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228741311·GC Initial™ Ti Shoulder Transpa ST-31, 20g

    SCENTED MENSTRUAL PAD

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    NUCLEOTOME

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    7.0MM TI SIDE-OPENING SCREW 45MM

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MNH·December 14, 2012

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·October 15, 2010

    LARGE SUTURECUT NEEDLE DRIVERINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 16, 2014

    Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1. Allura Xper FD10, Model Number: 722010. 2. Allura Xper FD10/10, Model Number: 722011. 3. Allura Xper FD20, Model Number: 722012. 4. Allura Xper FD20 Biplane, Model Number: 722013. 5. Allura Xper FD10 OR Table, Model Number: 722022. 6. Allura Xper FD20 OR Table, Model Number: 722023. 7. Allura Xper FD20 Biplane OR Table, Model Number: 722025.

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·December 18, 2024