BEUDAMED
    62 results · 39ms · Sources: EU EUDAMED, US FDA

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    PRISTINE SURGICAL LLC

    FDA registration
    PRISTINE SURGICAL LLC·2 products·🇺🇸 United States

    Summit Hi-Flow Cannula

    FDA UDI
    Pristine Surgical LLC·10860003634629·

    Summit Single Use Surgical Arthroscope

    FDA UDI
    Pristine Surgical LLC·10860003634605·

    Summit Imagine Processing Unit

    FDA UDI
    Pristine Surgical LLC·00860003634615·

    EVOLUTION® MP? CS INSERT SIZE 4 STANDARD 12MM LEFT

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code HRY·October 26, 2023

    EVOLUTION® MP? CS INSERT SIZE 4 STANDARD 12MM RIGH

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code HRY·October 25, 2023

    PDS II (POLYDIOXANONE) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAN·June 18, 2008

    PALACOS R 1X 40G SINGLE

    FDA Adverse Event
    Injury ·ZIMMER SURGICAL·Product code LOD·February 25, 2015

    FREESTYLE AORTIC ROOT BIOPROSTHESIS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·December 21, 2016

    JAWS NITINOL STAPLE SYSTEM

    FDA Adverse Event
    Malfunction ·PARAGON 28, INC.·Product code JDR·November 18, 2020

    UNKNOWN SUTURE PRODUCT

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·June 4, 2013

    PRIMARY TRITANIUM HEMI CLUSTER HOLE CUP 54MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·May 1, 2018

    SIZE 3 ACCOLADE II 127 DEG

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·May 2, 2018

    ORA SYSTEM WITH VERIFEYE MESSAGING

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code NCF·September 4, 2020

    FAST-FIX 360 CURVED NDL DELIVERY SYS

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code GAT·March 14, 2024

    LOGIC FEMORAL PS CEM LEFT SZ 3

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·May 11, 2026

    ATTUNE REVISION BROACH HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND 9616671·Product code LXH·July 18, 2018

    FOUNDATION KNEE

    FDA Adverse Event
    Injury ·ENCORE MEDICAL, L.P.·Product code JWH·April 17, 2014

    CONTINUUM TRILOGY IT LONGEVITY POLY LINER

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JDI·April 7, 2011

    TRIATHLON CR BEADED FEM #5R

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·November 2, 2015