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

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    SteriZign Signatur Device Protection System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DD tempMED

    FDA UDI
    Dental Direkt GmbH·EDDIK115201·DD tempMED are pre-colored dental milling blank...

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100769·FLIERINGA FIXATION RING 15MM

    SR MCP

    FDA UDI
    Stryker GmbH·00886385020907·S.R. MCP PHALANGEAL BROACH ASSEMBLY, XS

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071715202DC0·Custom Bayonet Curette #2/0 REV ANG DWN 8" working

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071715200D0·Custom Bayonet Curette #2/0 STR DWN

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071715201D0·Custom Bayonet Curette #2/0 ANG DWN

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071715202U0·Custom Bayonet Curette #2/0 REV ANG UP

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071715201UC0·Custom Bayonet Curette #2/0 ANG UP 8" working

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93071715200U0·Custom Bayonet Curette #2/0 STR UP

    ENSEAL TISSUE SEALING DEVICES MODEL: NSEAL514H-535H, NSEAL514RH-535RH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    RENOVO SUTURE ANCHORS, MODELS 100-2001 THRU 100-5502X

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REFOBACIN BONE CEMENT R 1X40-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 30, 2026

    REFOBACIN BONE CEMENT R 1X40-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·February 24, 2026

    OPTIPAC 80 REFOB PLUS BONE CMT-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·March 17, 2026

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DTQ·June 24, 2011

    STERRAD 100S STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·September 17, 2008

    REFOBACIN BONE CEMENT R 2X40G

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code MBB·March 12, 2026

    REFOBACIN BONE CEMENT R 2X20-3

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·February 11, 2026