BEUDAMED
    28 results · 21ms · Sources: EU EUDAMED, US FDA

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    FROSTED GLASS SLIDES

    FDA 510(k)
    FDA Class 1 ·Pathology

    Screwdriver

    FDA UDI
    ADLER ORTHO SPA·08052693626847·SCREWDRIVER 420B HEX 3.5 mm

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955930874·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955929779·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955931970·Percutaneous Transluminal Angioplasty Balloon C...

    DiMIM® Mini-Twin® Brackets

    FDA UDI
    Ortho Organizers, Inc.·00190707082147·DiMIM® Mini-Twin® .018 UL3 -2T 11A 0O

    T7

    FDA UDI
    STRYKER CORPORATION·07613327466126·Zippered Toga with Peel Away Face Shield

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971659·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172972274·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971642·

    7200 MA ECHO-OPHTHALMOSCOPE

    FDA 510(k)
    FDA Class 2 ·Radiology

    SL 803, SL 804, SL 807, SL 809, SL 506, SL 501, SL 805 AND SL 801 MECHANICAL WHEELCHAIRS

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    UNKNOWN DEPUY SZ 3 10MM PS TIB INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.-1818910·Product code JWH·May 20, 2014

    PLEXUR M

    FDA Adverse Event
    Injury ·OSTEOTECH, INC.·Product code MQV·November 1, 2012

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·June 4, 2015

    T5 Zipper Toga with Peel-Away Face Shield, (L/XL); Catalog number: 0400-820-100 Sterile personal protection garment

    FDA Enforcement
    Class II ·Terminated·Stryker Instruments Div. of Stryker Corporation·May 2, 2018

    SAFETY NEEDLE 25 X 1

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 4, 2018

    SAFETY NEEDLE 25 G X 1"

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 3, 2018

    SERIES A PAT THN 34 3 PEG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 12, 2022

    Boston Scientific Vesica Sling Kits with Drill-In Anchor System sterile, for single use only; Ref/Catalog No. 820-100, UPN Product No. (M0068201000).

    FDA Recall
    Terminated ·Boston Scientific Corp·Product code JDR·June 2, 2006