BEUDAMED
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    BruxZir Steel

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777631·LUMBAMED BASIC DORSAL STAYS M SILVER I

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·04026704417582·SPONGE NEURO STERILE XRAY 1/2X6"

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825002930·Steerable Diagnostic EP Catheter , LARGE 4.0, 4...

    N/A

    FDA UDI
    INNOVATIVE HEALTH LLC·10841898113369·Dynamic Tip Steerable Diagnostic EP Catheter 11...

    7000 CONNECTORS

    FDA UDI
    HANS RUDOLPH, INC.·00817136022178·CONN 35IDORG X 27IDORG 7000

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K100131101·IN-OVATION® C Base Rx 018 U3-3 CS HK

    PATIENT CIRCUITS

    FDA UDI
    Zoll Medical Corporation·00847946023201·CIRCUIT, MRI, VENT, SINGLE LIMB, INFANT

    PATIENT CIRCUITS

    FDA UDI
    Zoll Medical Corporation·10847946023208·CIRCUIT, MRI, VENT, SINGLE LIMB, INFANT

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K100131611·IN-OVATION® C Roncone 018 U3-3 CS HK

    Initia Total Hip System

    FDA UDI
    KYOCERA CORPORATION·04547898306303·STD LINER 32-66/70

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825002947·Steerable Diagnostic EP Catheter , LARGE 4.0, 4...

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780182115·Integra® Jarit® McBurney Thyroid Retractor

    QUICKSCREEN PRO MULTI DRUG SCREENING TEST, MODEL 9153 PAT04

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    VENUS UNIVERSAL LIGHT CURING COMPOSITE

    FDA 510(k)
    FDA Class 2 ·Dental

    LINER FOR METAL BACK GLENOID STANDARD

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·December 22, 2021

    DRACO

    FDA UDI
    HNM TOTAL RECON LLC·00841742121826·DRACO MetaFuse BLP Plate, Ti - (L)31mm, L

    RUNTHROUGH NS

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 9, 2017

    REVERSE #SHORT HUM. BODY 140°

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A·Product code MBF·November 11, 2022

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 30, 2019