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

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    Haemostasis Clips

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TRACHSEALTM ADULT TRACHEOSTOMY CLOSED SUCTION SYSTEM WITH NACL AMPOULES, 24 HOUR

    FDA UDI
    Intersurgical Incorporated·05030267153657·TRACHSEALTM ADULT TRACHEOSTOMY CLOSED SUCTION S...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180159143·PROTECTOR SLOOTED SCOPE MOUNTING SLEEVE FOR 5 M...

    3.5mm Proximal Tibia Plate 4 Holes Left

    FDA UDI
    mahe medical gmbh·EMAH20002410050·3.5mm Proximal Tibia Plate 4 Holes Left

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659349759·3.5mm Proximal Tibia Plate 4 Holes Left ...

    GAMBRO PRISMAFLEX AND GAMBRO PRISMAFLEX M60 & M100 SETS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Z-LINK CERVICAL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    9616026-2006-00240

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616026-2006-00244

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024041233·

    9616026-2006-00239

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    9616026-2006-00222

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    9616026-2006-00252

    FDA Adverse Event
    Other ·Product code FII·June 21, 2006

    9616026-2006-00245

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    9616026-2006-00253

    FDA Adverse Event
    Other ·Product code FII·June 21, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    9616026-2006-00221

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006