BEUDAMED
    25 results · 24ms · Sources: EU EUDAMED, US FDA

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    Surgical Green Laser System

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

    Syntec Osteo-plate and screw Fixation

    FDA UDI
    SYNTEC SCIENTIFIC CORPORATION·04712782853939·Cortex Screw Self-Tappingφ2.7 x L28mm

    NA

    FDA UDI
    Synthes GmbH·10886982144805·2.7MM CORTEX SCREW SELF-TAPPING 28MM

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113257·VITRECTOMY KNIFE 25GA (BX/5)

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A202828150·20mm H x 28mm W x 28mm L x 15 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A202828120·20mm H x 28mm W x 28mm L x 12 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A20282880·20mm H x 28mm W x 28mm L x 8 degrees ALIF

    XPS NITRO SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    OSTEOSET DBM PELLETS, MODEL 8600-48XX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 30, 2012

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 27, 2020

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code NIQ·September 5, 2006

    UNK

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·October 17, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code KDJ·July 2, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·April 8, 2021

    CD HORIZON SOLERA VOYAGER SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·May 27, 2024

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·August 20, 2025

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code KWP·August 20, 2025

    CD HORIZON® BALLAST¿ SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NKB·February 6, 2024