BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    Phototherapy System (OL-PDT950)

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

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517630384·CoRoent Ant TLIF Ti, 13x10x34mm 12°

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780183785·Integra® Jarit® Liston Bone Cutting Forceps, 7-...

    Cooley Pediatric Aortic Clamp 20cm

    FDA UDI
    Geister Medizintechnik GmbH·04057034061282·Cooley Pediatric Aortic Clamp 20cm

    LUMENIS FAMILY OF IPL SYSTEMS AND COMBINATION IPL/ND:YAG SYSTEMS

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

    SAUFLON CLARITI (SOMOFILCON A) SOFT (HYDROPHILIC) CONTACT LENS WITH UV BLOCKER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    TITANIUM HEXED UNISCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·July 20, 2020

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 21, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 1, 2011

    IFS

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·July 16, 2013

    Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x45 mm Catalog Number: 18965045S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.

    FDA Enforcement
    Class II ·Terminated·Stryker GmbH·June 24, 2020