BEUDAMED
    FDA Registration Active 🇮🇹 Italy

    ProCUT P/5 KIT

    Reg #: 1000391282 · FEI: 1000391282 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    50
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    MILESTONE S.r.l.
    Registration Number
    1000391282
    FEI Number
    1000391282
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Via Fatebenefratelli, 1/5
    City
    Sorisole Bergamo
    Country
    IT

    Owner / Operator

    Firm Name
    MILESTONE S.r.l.
    Operator Number
    10023724
    Address
    Via Fatebenefratelli, 1/5
    City
    Sorisole
    State
    Bergamo
    Postal Code
    24010
    Country
    IT

    Products

    Device Name Product Code
    Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use LXG

    Proprietary Names

    ProCUT P/5 KIT Foam boards XXL/5 140mm Foam Boards P/5 40mm eGROSS pro-x CUTMATE 4 forceps Foam boards XL/5 100mm Dome Complete P/5 40mm ProCUT XXL/5 station ProCUT P/5 TissueSAFE SM-SPACER 2MM Dome complete XL/5 100mm eGROSS CheckLITE ROSESTATION Dome complete XXL/5 140mm ProCUT XL/5 KIT LeanSTATION Bx CUTMATE 3mm forceps tissue block ProCUT XXL/5 KIT Dome complete XL/5 120mm Dome complete XL/5 80mm CUTMATE 2mm forceps tissue block Foam boards XL/5 80mm WorkSTATION CUTMATE Starter KIT Dome complete XXL/5 120mm Foam boards XL/5 60mm ProCUT Starter KIT SealSAFE CUTMATE Calibration device ProCUT XL/5 Foam boards XL/5 120mm RoseSTATION ProCUT XL/5 station WorkSTATION Bx CUTMATE 2,3,4, 2/3/4mm WorkSTATION 140 CUTMATE 4mm forceps tissue block ProCUT P/5 Station Foam Boards P/5 60mm Dome complete XXL/5 100mm Dome complete XL/5 60mm Foam boards XXL/5 100mm ProCUT XXL/5 Dome Complete P/5 60mm WorkSTATION Bx 140 CUTMATE 2/3/4mm forcep tissue block Foam boards XXL/5 120mm ULTRASAFE

    Establishment Types

    Manufacture Medical Device