BEUDAMED
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    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61491·Cervical Spine Interbody Device. 14 x 16mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61201·Cervical Spine Interbody Device. 12 x 14mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61481·Cervical Spine Interbody Device. 14 x 16mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61421·Cervical Spine Interbody Device. 14 x 16mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61251·Cervical Spine Interbody Device. 12 x 14mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61271·Cervical Spine Interbody Device. 12 x 14mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61461·Cervical Spine Interbody Device. 14 x 16mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61221·Cervical Spine Interbody Device. 12 x 14mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61281·Cervical Spine Interbody Device. 12 x 14mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61411·Cervical Spine Interbody Device. 14 x 16mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61451·Cervical Spine Interbody Device. 14 x 16mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61471·Cervical Spine Interbody Device. 14 x 16mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61211·Cervical Spine Interbody Device. 12 x 14mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61401·Cervical Spine Interbody Device. 14 x 16mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61291·Cervical Spine Interbody Device. 12 x 14mm foot...

    Addivation Medical Cervical Interbody Device

    FDA UDI
    ADDIVATION MEDICAL, LLC·B804AOCS61261·Cervical Spine Interbody Device. 12 x 14mm foot...

    YOUNG DH Dry Heat Indicators, PRESSURE SENSITIVE LABELS with COLOR INDICATOR STRIP, REF 116312 Intended for use by a health care provider to accompany products being sterilized through a sterilization procedure and to monitor one or more parameters of the sterilization process.

    FDA Recall
    Open, Classified ·Young Dental Mfg Co I LLC·Product code JOJ·December 29, 2021

    Sigma Spectrum VOLUMETRIC INFUSION PUMP, with or without Master Drug Library, Part Number 35700 -- Common/Classification Name: Infusion Pump -- Class 2 medical device -- SIGMA LLC, Medina, NY 14103 Product Usage: The Spectrum Infusion Pump is intended to be used for the controlled administration of intravenous fluids. These fluids may include blood, blood products or mixtures of pharmaceutical drugs for required patient therapy. The Spectrum is used in conjunction with legally marked intravenous administration sets and medications provided by the user. The Master Drug Library is a software package that will add additional features to the Spectrum Infusion Pump. The Master Drug Library will permit electronic communications with the Spectrum pump and other external peripheral devices. The intended use of the Spectrum pump includes common drug error prevention, through the stand alone settings features of the pump. This includes drug parameter limits and associated drug name identification. With the Master Drug Library, the intended use is to reduce user errors associated with drug selection, drug dose rates, drug dose concentrations, and patient identification associated with the prescribed drug.

    FDA Enforcement
    Class I ·Terminated·Baxter Healthcare Corporation·June 20, 2012

    Nimbus Administration Set, REF HS-004, UDI # 00817170020031 Product Usage: Administer fluids/medication from a container to a patient through a needle or a catheter.

    FDA Recall
    Terminated ·InfuTronix LLC·Product code FRN·May 28, 2019

    regard Clinical Packaging Solutions, HT00376I - SPECIAL PROCEDURE, Item Number 800223009

    FDA Recall
    Open, Classified ·ROi CPS LLC·Product code OEQ·July 24, 2024