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

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    VITEK 2 AST-Gram Positive Cefoxitin Screen

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526159600·PROTECT.GENU KNEE SUPPORT GRAY V

    Ecosite Elements

    FDA UDI
    DMG Chemisch-Pharmazeutische Fabrik GmbH·EDMG2208051·Ecosite Elements is a light-curing, esthetic, r...

    Zavation

    FDA UDI
    Zavation LLC·00842166132979·Ti3Z CIF 14mmx16mmx5mm -8 deg

    ZAVATION

    FDA UDI
    Zavation LLC·00842166105065·CIF 14x16, 8 deg, -05

    ShurFit Interbody Device

    FDA UDI
    PRECISION SPINE, INC.·00840019911412·Narrow PLIF Cage Peek 5 degree 22 x 8 X 14

    ShurFit Interbody Device

    FDA UDI
    PRECISION SPINE, INC.·00840019911399·Narrow PLIF Cage Peek 5 degree 22 x 8 X 12

    ShurFit Interbody Device

    FDA UDI
    PRECISION SPINE, INC.·00840019911375·Narrow PLIF Cage Peek 5 degree 22 x 8 X 10

    ShurFit Interbody Device

    FDA UDI
    PRECISION SPINE, INC.·00840019911405·Narrow PLIF Cage Peek 5 degree 22 x 8 X 13

    ShurFit Interbody Device

    FDA UDI
    PRECISION SPINE, INC.·00840019911429·Narrow PLIF Cage Peek 5 degree 22 x 8 X 15

    ShurFit Interbody Device

    FDA UDI
    PRECISION SPINE, INC.·00840019911382·Narrow PLIF Cage Peek 5 degree 22 x 8 X 11

    ShurFit Interbody Device

    FDA UDI
    PRECISION SPINE, INC.·00840019911436·Narrow PLIF Cage Peek 5 degree 22 x 8 X 16

    ShurFit Interbody Device

    FDA UDI
    PRECISION SPINE, INC.·00840019911351·Narrow PLIF Cage Peek 5 degree 22 x 8 X 8

    CR Peg Multi Tool

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215127558·

    ShurFit Interbody Device

    FDA UDI
    PRECISION SPINE, INC.·00840019911368·Narrow PLIF Cage Peek 5 degree 22 x 8 X 9

    Neocis Guidance System (NGS) with Patient Splints

    FDA 510(k)
    FDA Class 2 ·Dental

    PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 30, 2024

    I-STAT EC8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code CHL·October 27, 2022

    VANTEX CENTRAL VENOUS CATHETER WITH OLIGON MATERIAL WITH OR WITHOUT AMC THROMBOS

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code DQO·October 30, 2008