BEUDAMED
    28 results · 30ms · Sources: EU EUDAMED, US FDA

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    MACROPORE HYDROSORB SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sure-Vue RSV Test

    FDA UDI
    SA SCIENTIFIC, LTD.·00780311000578·Sure-Vue® RSV antigen test kit is a visual and ...

    AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 105mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665010077·

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867522459·Cannulated Canc Screw,36mm Thd,7.0x105mm

    MOSS MIAMI 6.35MM ROD SYSTEM PEDICLE AND LAMINAR HOOKS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SUTURTEK FASTCLOSE FASCIA CLOSURE DEVICE

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

    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

    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

    HATCP STEM POR TIB PLT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·March 5, 2024

    9616026-2006-00221

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

    PRISMAFLEX SETS (M)

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDI·May 13, 2024