BEUDAMED
    28 results · 22ms · Sources: EU EUDAMED, US FDA

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    PDE PHOTODYNAMIC EYE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776184490·T - Handle Bone Hook Hook

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902096396·GUIDE 9110480 TREPHINE TPRD 18MM

    JOBST ActiveWear

    FDA UDI
    BSN MEDICAL, INC.·00035664104801·ACTIVE WEAR 15-20 MM HG KNEE HIGH CLOSED TOE ME...

    NA

    FDA UDI
    Smith & Nephew, Inc.·00885556008324·T-HANDLED BONE HOOK 1 IN

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306816765·Heiss Self-Retaining Skin Retractor, Blunt Blad...

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529583170·Apex Femoral Nail PF Left Ø 11.0 x 480mm

    NATRELLE Silicone-Filled Breast Implants

    FDA UDI
    Allergan, Inc.·10888628002289·NATRELLE Style 110-480 Moderate profile BIOCELL...

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529587109·Apex Femoral Nail GT Right Ø 11.0 x 480mm

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529586201·Apex Femoral Nail GT Left Ø 11.0 x 480mm

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529585303·Apex Femoral Nail PF Right Ø 11.0 x 480mm

    VERSAFITCUP CC CUP IMPACTOR

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·March 27, 2014

    RADIAL-EMITTING SHAPED FIBER OPTIC DELIVERY SYSTEM

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

    ROTA-TRACH TRACHEOSTOMY TUBE MODEL ROTA-TRACH

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TAPERLOC COMPLETE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·February 9, 2026

    TPRLC 133 MP TYPE1 BM SO 9.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 27, 2018

    BioMend Absorbable Collagen Membrane BioMend¿ Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue regeneration procedures in periodontal defects to enhance regeneration of the periodontal apparatus.

    FDA Enforcement
    Class II ·Terminated·Integra LifeSciences Corporation·May 22, 2013

    MEDPOR IMPLANT

    FDA Adverse Event
    Injury ·STRYKER CRANIOMAXILLOFACIAL GEORGIA·Product code FWP·June 1, 2011

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

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

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·September 23, 2014