BAYER MEDICAL CARE INC.

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 33 건

  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: (Lot serial: )
  • 제품 설명
    CONTINUUM MR COMPATIBLE INFUSION SYSTEM
  • 모델명 / 제조번호(시리얼번호)
    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:
  • 제품 설명
    OVERHEAD COUNTERPOISE SYSTEM II
  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: INT CSS (Lot serial: >10. Contact Manufacturer.)
  • 제품 설명
    Medrad Intego PET Infusion System - Source Administration Sets
  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: MRXP 200 (Lot serial: Serial Number 100054)
  • 제품 설명
    MRXPERION MR INJECTION SYSTEM
  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: MRXP 200 (Lot serial: 100166); Model Catalog: MRXP 200 (Lot serial: 100104); Model Catalog: MRXP 200 (Lot serial: 100085)
  • 제품 설명
    MRXPERION MR INJECTION SYSTEM
하나 더 28 건 더

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 11 건

데이터에 대해 더 자세히 알아보기 여기

  • 제조사 모회사 (2017)
  • 제조사 의견
    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
  • 제조사 모회사 (2017)
  • Source
    MHSIDCCCDMIS
  • 제조사 모회사 (2017)
  • Source
    VNSAWH
하나 더 6 건 더