BEUDAMED
    73 results · 20ms · Sources: EU EUDAMED, US FDA

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    ZIMMER PATIENT SPECIFIC INSTRUMENTS PLANNER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526749733·MANUMED RFX FRACTURE BRACE, RIGHT SIZE 1

    EVOTECH™

    FDA UDI
    ADVANCED STERILIZATION PRODUCTS SERVICES INC.·10705037048168·Channel Connector Tube, Orange, DB-HLD

    Baby Gorilla/Gorilla Plating System

    FDA UDI
    Paragon 28, Inc.·00889795035042·MTP Spin Guard Male Reamer Protector Sleeve, 23mm

    IMMULITE 2000 DIGOXIN, MODELS L2KDI2 (200 TESTS) AND L2KDI6 (600 TESTS)

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SILK'N FX

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

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230100110·11mm SM FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230100130·13mm SM FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230100140·14mm SM FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230100070·7mm SM FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230100090·9mm SM FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230100120·12mm SM FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230100100·10mm SM FP Lordotic Implant, HiJAK™ Stand Alone

    HiJAK™ Stand Alone

    FDA UDI
    ATLAS SPINE, INC.·M68111230100080·8mm SM FP Lordotic Implant, HiJAK™ Stand Alone

    ENDOWRIST FENESTRATED BIPOLAR FORCEPS

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code NAY·March 5, 2024

    UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·May 14, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·September 23, 2014

    LIFESTENT VASCULAR STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHIK·Product code NIP·May 23, 2011

    TL PEDICLE SCREW DIA. 6,5 LG 50

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019