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

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    MODIFICATION TO EXACTECH ACUMATCH INTEGRATED HIP SYSTEM, M-SERIES HIGH OFF-SET NECK SEGMENT, M-SERIES LOW OFF-SET NECK S

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Axcent Acrylics

    FDA UDI
    GARRECO, LLC·D79330101200·Repair Clear 20lb

    SCANLAN® Pincap® orthopedic pin protectors

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159002348·SCANLAN® Pincap® orthopedic pin protectors - Pi...

    Santis Pre Bent Rod 5.5mmx120mm

    FDA UDI
    Lanterna Medical Technologies GmbH·07640159550679·Santis Pre Bent Rod 5.5mmx120mm

    Soft-Form™ Thermo Plastic External Nasal Splint

    FDA UDI
    INVOTEC INTERNATIONAL, INC.·00818501022458·Soft-Form™ Thermo Plastic External Nasal Splint...

    Snap On Spherz

    FDA UDI
    Izi Medical Products, LLC·00815212021442·

    Snap on Spherz

    FDA UDI
    Izi Medical Products, LLC·00815212024405·

    GMA 2.0 Pedicle Screw System

    FDA UDI
    GRAFTON MEDICAL ALLIANCE, INC.·00810021380322·PRE-BENT ROD, ø5.5 X 120

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C30430101200·PEEK PLIF Spacer, 30 x 10 x 12mm, 0 deg

    Savant Lumbar Interbody Fusion System

    FDA UDI
    CURITEVA, INC.·B648C31430101200·Titanium PLIF Spacer, 30 x 10 x 12mm, 0 deg

    Ti-Fix OLIF Spacer

    FDA UDI
    Tyber Medical, LLC·M695P30101200·Ti-Fix OLIF Spacer 30 x 10 x 12 (mm) x 0 °

    SANTIS™ PRE BENT ROD 5.5mm X120mm -STERILE

    FDA UDI
    Lanterna Medical Technologies GmbH·07640159551799·SANTIS™ PRE BENT ROD 5.5mm X120mm -STERILE

    ENVOY PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRO-TORQ

    FDA 510(k)
    FDA Class 1 ·Dental

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·June 29, 2018

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 13, 2025

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

    EYE SURGERY STRETCHER OBS

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·March 1, 2011

    ENDO CATCH II 15MM SPECIMEN POUCH

    FDA Adverse Event
    Malfunction ·SANTO DOMINGO - USS·Product code GCJ·March 10, 2008

    INTELLIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·May 29, 2020