BAYER MEDICAL CARE INC.

33 devices in the database

  • Model / Serial
    Model Catalog: (Lot serial: )
  • Product Description
    CONTINUUM MR COMPATIBLE INFUSION SYSTEM
  • Model / Serial
    Model Catalog: OCS 135A (Lot serial: 3010552); Model Catalog: OCS 155A (Lot serial: 3010552); Model Catalog: OCS 115A (Lot serial: 3010552); Model Catalog: OCS 155A (Lot serial: 3010551); Model Catalog: OCS 135A (Lot serial: 3010551); Model Catalog: OCS 125A (Lot serial: 3010551); Model Catalog: OCS 115A (Lot serial: 3010551); Model Catalog: OCS 155A (Lot serial: 3010550); Model Catalog: OCS 135A (Lot serial: 3010550); Model Catalog: OCS 125A (Lot serial: 3010550); Model Catalog: OCS 115A (Lot serial: 3010550); Model Catalog: OCS 155A (Lot serial: 3010549); Model Catalog: OCS 135A (Lot serial: 3010549); Model Catalog: OCS 125A (Lot serial: 3010549); Model Catalog: OCS 115A (Lot serial: 3010549); Model Catalog: OCS 155A (Lot serial: 3010548); Model Catalog: OCS 135A (Lot serial: 3010548); Model Catalog: OCS 125A (Lot serial: 3010548); Model Catalog: OCS 115A (Lot serial: 3010548); Model Catalog: OCS 155A (Lot serial: 3010547); Model Catalog: OCS 135A (Lot serial: 3010547); Model Catalog: OCS 125A (Lot serial:
  • Product Description
    OVERHEAD COUNTERPOISE SYSTEM II
  • Model / Serial
    Model Catalog: INT CSS (Lot serial: >10. Contact Manufacturer.)
  • Product Description
    Medrad Intego PET Infusion System - Source Administration Sets
  • Model / Serial
    Model Catalog: MRXP 200 (Lot serial: Serial Number 100054)
  • Product Description
    MRXPERION MR INJECTION SYSTEM
  • Model / Serial
    Model Catalog: MRXP 200 (Lot serial: 100166); Model Catalog: MRXP 200 (Lot serial: 100104); Model Catalog: MRXP 200 (Lot serial: 100085)
  • Product Description
    MRXPERION MR INJECTION SYSTEM
28 more

11 manufacturers with a similar name

Learn more about the data here

  • 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
  • Manufacturer Parent Company (2017)
  • Source
    BAM
  • Manufacturer Parent Company (2017)
  • Source
    MHSIDCCCDMIS
  • Manufacturer Parent Company (2017)
  • Source
    SMPA
  • Manufacturer Parent Company (2017)
  • Source
    VNSAWH
6 more