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

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    Promisemed Fine Biopsy Needle

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

    Grifols Wash Solution B

    FDA UDI
    DIAGNOSTIC GRIFOLS SA·08436583731895·Grifols Wash Solution B is used for internal wa...

    Grifols Wash Solution B

    FDA UDI
    DIAGNOSTIC GRIFOLS SA·08437014205893·Grifols Wash Solution B is used for internal wa...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180124493·5MM DIA., 36CM, INSULATED SPATULA TIP ELECTRODE...

    MODIFICATION TO: ABBOTT VASCULAR SUTURE ANASTOMOSIS DEVICE

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

    LIFESHIELD VISION INFUSION SET WITH PRE-PIERCED RESEAL

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EXTENSION SET WITH T-CONN. SL

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·October 3, 2013

    HIRES 90K

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS LLC·Product code MCM·October 23, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 16, 2011

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 9, 2013

    SNAPLOC WIRE GUIDE LOCKING DEVICE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code ODC·December 18, 2024

    SNAPLOC WIRE GUIDE LOCKING DEVICE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code ODC·December 16, 2024

    HEMOSPHERE FORESIGHT MODULE

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code MUD·February 26, 2026

    SNAPLOC WIRE GUIDE LOCKING DEVICE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code ODC·May 20, 2024

    SNAPLOC WIRE GUIDE LOCKING DEVICE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code ODC·June 10, 2024

    SNAPLOC WIRE GUIDE LOCKING DEVICE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code ODC·December 13, 2024

    SNAPLOC WIRE GUIDE LOCKING DEVICE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code ODC·November 11, 2024

    SNAPLOC WIRE GUIDE LOCKING DEVICE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code ODC·November 11, 2024

    MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

    SNAPLOC WIRE GUIDE LOCKING DEVICE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code ODC·November 12, 2024