BEUDAMED
    25 results · 61ms · Sources: EU EUDAMED, US FDA

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    SPINAL EPIDURAL NEEDLES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SW

    FDA UDI
    SW SAFETY SOLUTIONS INC.·00616489004059·PowerChem Neoprene Exam Gloves, Extra Large

    Batrik Blue Cloud-Gel Anti-Fatigue Floor Mats

    FDA UDI
    Batrik Medical Manufacturing Inc·00690521011625·Blue Cloud-GelTM Anti-Fatigue Mat, 18" x 24" (4...

    DriDye 405

    FDA UDI
    AWARENESS TECHNOLOGY, INCORPORATED·00850229007195·Analyzer Quality Control

    Battalion

    FDA UDI
    ALPHATEC SPINE, INC.·00840967188812·Battalion, LLIF Trial, 0°, 24 mm Wide, 05 mm X ...

    INTERCURE LTD. RESPI-LOW

    FDA 510(k)
    FDA Class 2 ·Neurology

    BOLUSPRO ULTRA

    FDA 510(k)
    FDA Class 2 ·Radiology

    COAPTITE

    FDA Adverse Event
    Other ·BIOFORM MEDICAL, INC.·Product code LMH·October 13, 2006

    NI

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·May 13, 2022

    VENTED MICRO VOL.INLET, N/S

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·March 28, 2022

    APTIMA SARS COV-2

    FDA Adverse Event
    Malfunction ·HOLOGIC, INC.·Product code OJR·July 21, 2022

    VALVE SET, EM2400

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·April 7, 2022

    VALVE SET, EM2400

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·August 8, 2022

    DEXTRUS 4136

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVN·March 13, 2013

    LCS TEX FEM LG+ RT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code NJL·February 18, 2011

    CONTAK RENEWAL 4

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code NIK·February 7, 2008

    250 ML TPN BAG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·May 21, 2021

    EXACTA-MIX 2400 COMPOUNDING SYSTEM

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code NEP·February 27, 2023

    ***Processed at: Regeneration TECHNOLOGIES, INC. Alachua, FL, USA 32615***Distributed by: SpinalGraft Technologies, LLC 4340 Swinnea Road STE 39 Memphis, TN 38118***OSTEOFIL DBM Paste, 5cc Tissue ID: 321933 Reorder: 002405 Lot #(Donor ID): 101050353 Expiration: 02/21/2013***STERILE***" Bone Void Filler used in spinal surgery.

    FDA Recall
    Terminated ·RTI Biologics, Inc.·Product code MQV·April 9, 2011

    Remel Chocolate Agar, catalog #01301, containing 15 plates/pkg, for in-vitro diagnostic use. The firm name on the label is Remel, Lenexa, KS.

    FDA Recall
    Terminated ·Remel, Inc.·Product code KZI·September 27, 2004