DxH 500

Manufacturer

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ

29 devices with a similar name

Learn more about the data here

  • Model / Serial
    Model Catalog: B40601 (Lot serial: AZ120651); Model Catalog: B40601 (Lot serial: AZ120636); Model Catalog: B40601 (Lot serial: BA070451); Model Catalog: B40601 (Lot serial: BA060399); Model Catalog: B40601 (Lot serial: AZ120657); Model Catalog: B40601 (Lot serial: AZ120656); Model Catalog: B40601 (Lot serial: AZ120655); Model Catalog: B40601 (Lot serial: AZ110582); Model Catalog: B40601 (Lot serial: BA070450); Model Catalog: B40601 (Lot serial: AZ060306); Model Catalog: B40601 (Lot serial: 1.0.2 and 1.1); Model Catalog: B40601 (Lot serial: AZ030171); Model Catalog: B40601 (Lot serial: BA060398)
  • Product Description
    DXH 500 OPEN-VIAL HEMATOLOGY SYSTEM
  • Manufacturer
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