Device Recall Terumo Custom Kit

Manufacturer

  • Manufacturer Address
    Terumo Cardiovascular Systems Corp, 28 Howe St, Ashland MA 01721-1305
  • Manufacturer Parent Company (2017)
  • Source
    USFDA

11 devices with a similar name

Learn more about the data here

  • Model / Serial
    Lots: ME19, MF03
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distribution USA and Canada
  • Product Description
    Terumo Cardiovascular Procedure Kit Custom || MP4, 4:1, PRELIEF, W/RECIRC, COND / PUMP & TABLE PACK || P/N 65503/70881-02
  • Manufacturer
  • Model / Serial
    Lots: ME19, ME26
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distribution USA and Canada
  • Product Description
    Terumo Cardiovascular Procedure Kit Custom || 8:1 CARDIOPLEGIA SET || P/N 70608-01
  • Manufacturer
  • Model / Serial
    Lots: MD22
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distribution USA and Canada
  • Product Description
    Terumo Cardiovascular Procedure Kit Custom || X-COATED ADULT PRESTIGE PACK || P/N 71544-01
  • Manufacturer
  • Model / Serial
    Lots: MF03
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distribution USA and Canada
  • Product Description
    Terumo Cardiovascular Procedure Kit Custom || ADULT PACK || P/N 71546-01
  • Manufacturer
  • Model / Serial
    Lots: ME26
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distribution USA and Canada
  • Product Description
    Terumo Cardiovascular Procedure Kit Custom || PERFUSION TUBING PACK || P/N 71733
  • Manufacturer
6 more