BEUDAMED
    24 results · 22ms · Sources: EU EUDAMED, US FDA

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    HIGH SILVER CONVENTIONAL

    FDA 510(k)
    FDA Class 2 ·Dental

    APC™ II Unitek™ Mini Uni-Twin

    FDA UDI
    3M UNITEK CORPORATION·00652221061836·Mini Uni-Twin(TM) Bracket APC(TM) II LR3 -7T/6A...

    Midway Select

    FDA UDI
    MIDWAY DENTAL SUPPLY, LLC·10843717104473·Stainless Steel H Files (Hand), Size # 60, Leng...

    APC™ PLUS Unitek™ Mini Uni-Twin

    FDA UDI
    3M UNITEK CORPORATION·00652221092854·Mini Uni-Twin(TM) Bracket APC(TM) PLUS LR3 -7T/...

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036159795·

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036284435·

    3M™ Unitek™ Uni-Twin™

    FDA UDI
    3M UNITEK CORPORATION·00652221015921·Mini Uni-Twin(TM) Bracket LR3 -7T/6A Hk .018 5/Pk

    SCREENERS METHAMPHETAMINE TEST, DRUGSCREEN DIP METHAMPHETAMINE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    3M RELY X VENEER CEMENT TRY-IN PASTER

    FDA 510(k)
    FDA Class 2 ·Dental

    DRACO

    FDA UDI
    HNM TOTAL RECON LLC·00841742122335·DRACO MetaFuse MTP Plate, Ti - (L)52mm, L

    B-P TOTAL SHOULDER SYSTEM

    FDA UDI
    ENDOTEC, INC.·00814193025067·B-P SHOULDER GLENOID BEARING SIZE 4, 0 MM THICK...

    SMR GLENOSPHERE Ø 36MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·September 20, 2022

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 31, 2007

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 26, 2013

    EON RECHARGEABLE IPG

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·February 8, 2011

    CONTINUUM ACETABULAR SHELL WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 7, 2018

    KINECTIVE TECHNOLOGY MODULAR NECK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 7, 2018

    NEUTRAL LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·June 7, 2018

    SELF TAPPING BONE SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 7, 2018

    EB EXC GRN 8X18IN 0 S/A CT-1 CR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAT·March 13, 2020