Penlon, Ltd.

3 devices in the database

  • Model / Serial
    All lots with expiration dates between August 2011 and August 2016.
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA (nationwide) in the countries of Belgium, France, Greece, Ireland, Italy, Lithuania, Netherlands, Norway, Portugal, Switzerland, Canada, China, Hong Kong and Malaysia.
  • Product Description
    Crystal Metal Disposable Blades size Mac 4 (part number 50674, 50674/F, 50674/BMI) and Mac 3 (part numbers 50675, 50675/F, 50675/BMI) || Product Usage: Disposable laryngoscope blades.
  • Model / Serial
    All; recalled products are traced by serial numbers D0312-XXXX to D1112-XXXX.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA including FL, KY, PA, ND, MN, IL, NJ, TX, TN, and VA. Internationally to Belgium, China, Czech Republic, France, Germany, Switzerland, Australia, Finland, Holland, Lithunia, Malta, Poland, and Slovakia.
  • Product Description
    Delta Vaporizer || An anesthetic vaporizer is a device used to vaporize liquid anesthetic and deliver a controlled amount of the vapor to the patient.
  • Model / Serial
    None
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA (nationwide) and the countries of Peru, Uganda, Kenya, Malaysia, Poland, Saudi Arabia, United Arab Emirates, Philippines, Equador, and Thailand
  • Product Description
    Anesthesia Machines (digital display assembly); || A gas machine for anesthesia is a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation.

One manufacturer with a similar name

Learn more about the data here

  • Manufacturer Address
    Penlon, Ltd. (Fmly East Healthcare), Abingdon Science Park, Barton Lane, Abingdon United Kingdom
  • Manufacturer Parent Company (2017)
  • Source
    USFDA