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

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    Identity Imprint Knee Replacement System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BENT HOHMANN RETRACTOR

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·October 30, 2019

    BENT HOHMANN RETRACTOR

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·October 30, 2019

    NA

    FDA UDI
    MAKO SURGICAL CORP.·00848486031909·BENT HOHMANN RETRACTOR

    BENT HOHMANN RETRACTOR

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·August 7, 2018

    BENT HOHMANN RETRACTOR

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·August 7, 2018

    BENT HOHMANN RETRACTOR

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·August 7, 2018

    BENT HOHMANN RETRACTOR

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·August 7, 2018

    BENT HOHMANN RETRACTOR

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·August 7, 2018

    BENT HOHMANN RETRACTOR

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·September 12, 2019

    BENT HOHMANN RETRACTOR

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·November 15, 2019

    BENT HOHMANN RETRACTOR

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·November 15, 2019

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319706671·Desmarres Chalazion Forceps 3-1/2" (8.8cm), sma...

    Adler Instrument Company

    FDA UDI
    Adler, Inc.·00810123202836·KNIFE HDL NO 3KL RND 5-7/8

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210151111·Resolve® Ceramic R018 UL 5-5 CS BC HK

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210151811·Resolve® Ceramic M018 UL 5-5 CS BC HK

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210151121·Resolve® Ceramic R018 UL 5-5 CS HK/MBT 4-5

    Y2000 POCKET RESCUE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PUSH-ON NEEDLE 30GX8MM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PLUS SL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS AG·Product code KWY·October 23, 2008