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

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    VITEK 2 AST-Gram Positive Delafloxacin (<=0.015 - >=1 µg/mL)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825003456·Diagnostic EP Catheter, Cournand curve, 4 elect...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694016223·1.2mm Plate Holder

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180103023·BIPOLAR RF CABLE WITH ELMED (DIN) INSTRUMENT CO...

    iSmile

    FDA UDI
    Ismile Dental Products, Inc.·00816419021402·VP Micro Brush Applicator Superfine White

    WalkAide

    FDA UDI
    INNOVATIVE NEUROTRONICS, INC.·10858184006458·WalkAide Oval Velcro Electrode, 1.5" x 3.25", 1...

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756318648·200 ML CT PK FOR FRT LD INJ

    MODEL 733HC GRAVITY/VACUUM STEAM STERILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LATERAL PIVOT INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 24, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

    RESERVOIR 1.8ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·July 1, 2013

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·November 8, 2021

    Tibial Tray Nonporous A Size 2; Model # PN 162-1200-A; Material: Ti6Al4V.

    FDA Enforcement
    Class II ·Ongoing·Ortho Development Corporation·May 13, 2020

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 28, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 4, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 21, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 25, 2021