BEUDAMED
    31 results · 39ms · Sources: EU EUDAMED, US FDA

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    SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092103586·Straumann® TL WN-compatible Engaging Gold/Plast...

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950018420·FORCEP STERILIZING UNIVERSAL 8" 20CM

    365 by Whole Foods Market

    FDA UDI
    CORMAN SPA·00099482522902·365 Organic Cotton Tampons with Applicator - Su...

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001320·artVeneer life lower anteriors, UBXL, C1

    DISPOSABLE TIPS

    FDA UDI
    DiaDent Group International·08806383561921·DISPOSABLE SYRINGE TIPS

    Rampart One Lumbar Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7401001320·Trial 12mm L 8°

    SONOS AIRES 600 (SA-600)

    FDA 510(k)
    FDA Class 2 ·Radiology

    8100 VITAL SIGNS MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    APTIMA COMBO 2 ASSAY

    FDA Adverse Event
    Injury ·HOLOGIC, INC.·Product code LSL·March 7, 2025

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·November 19, 2024

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    NEOBLUE

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·September 26, 2017

    NEOBLUE

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·September 26, 2017

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece, & Alvarado II Base Plate and Foot Piece: Alvarado Foot Piece: Item Number: 00-1320-010-00 Alvarado Knee Holder Base Plate Assembly: Item Number: 00-1320-011-00 Alvarado II Foot Piece: Item Number: 00-1320-210-00 Alvarado II Base Plate: Item Number: 00-1320-211-00 Product Usage: This device is designed to hold the patient s knee in the selected position during surgery. The Alvarado Knee Holder includes a Base Plate assembly with two rows of slotted hooks. These rows extend upward from the base plate for a sufficient length to provide adequate selective adjustment. A Foot Piece is mounted on an alignment rod that is pivotally engaged into the hook portion of the slots.

    FDA Recall
    Terminated ·Zimmer Surgical Inc·Product code JEB·April 16, 2019

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015