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

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    Tinnitus Sound Generator Module

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Oticon

    FDA UDI
    Oticon A/S·05707131285904·H15V2, RITE 312 WL DBL

    BD

    FDA UDI
    PRYOR PRODUCTS·00761887002111·HEX BASE SNGL POLE/RAKE TOP

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100196·MCINTYRE SPECULUM OPEN WIRE

    ESI

    FDA UDI
    FTT MEDICAL, INC.·B3961501710·CCF HIRSCHMAN ANOSCOPE, 15/16" DIAMETER x 2-3/4...

    Tibial Keel Punch : SIZE 1

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215073985·

    TIBIAL INSERT IMPACTOR TIP

    FDA Adverse Event
    Malfunction ·CONFORMIS, INC.·Product code OOG·April 28, 2017

    Orthopedic Instruments

    FDA UDI
    GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258662817·

    NOBELPROCERA ZI ABUTMENT THOMMEN PLATFORMS

    FDA 510(k)
    FDA Class 2 ·Dental

    IT NASAL MASK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·July 21, 2017

    FASTTAKE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·July 19, 2002

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 19, 2023

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OZO·April 2, 2020

    T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 30, 2020

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 23, 2023

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 6, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 6, 2011

    SYNCHROMED II

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·September 3, 2008

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 20, 2013