BEUDAMED
    18 results · 28ms · Sources: EU EUDAMED, US FDA

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    SAM FACIAL IMPLANT

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

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295235675·P.F.C. SIGMA POSTERIOR-LIPPED TIBIAL INSERT TRI...

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690190684·+1/+3 Distal Cutting Block

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024158146·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024158139·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024158122·

    C-STEM

    FDA UDI
    DEPUY (IRELAND)·10603295235682·C-STEM VOID CENTRALISER 10mm

    RIALTO(TM) SI Fusion System, Medtronic Reusable Instruments for Use with the IPC(TM) Powerease(TM) System, and Medtronic Navigated Manual Reusable Instruments for use with the StealthStation(TM) and IPC(TM) Powerease(TM) Systems

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FUNCTIONAL ANAESTHETIC DISCOGRAPHY (FAD) CATHETER SYSTEM, MODEL D01A ; INTRODUCER NEEDLE, MODEL D01B

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·May 5, 2023

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 22, 2023

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 22, 2023

    PROXIMATE I L S INTRALUMINAL STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code GAG·September 13, 1996

    2 FR PER-Q-CATH PLUS PICC WITH STYLET, BASIC

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code LJS·February 8, 2013

    UNKNOWN T72 TIBIAL INSERT TRIAL

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·December 21, 2010

    UV FLASH TRANSFER SETS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 28, 2014

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 26, 2023

    Medtronic INTREPID Spinal System SPACER, 32X23, 12 DEG, Size: 10MM, Part Number: REF 7961210; 12MM, REF 7961212; 14MM, REF 7961214; 16MM, REF 7961216; 18MM, REF 7961218; 20MM, REF 7961220; Rx only, STERILE R The INTREPID Spinal System is indicated for use with autogenous bone graft in patients with degenerative disc disease.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code MAX·February 6, 2009