|
|
|
|
||||
|
|
||||||
|
|
820.170
Installation.
(a) Each
manufacturer of a device requiring installation shall establish and maintain
adequate installation and inspection instructions, and where appropriate test
procedures. Instructions and procedures shall include directions for ensuring
proper installation so that the device will perform as intended after
installation. The manufacturer shall distribute the instructions and
procedures with the device or otherwise make them available to the person(s)
installing the device. (b) The person
installing the device shall ensure that the installation, inspection, and any
required testing are performed in accordance with the manufacturer`s
instructions and procedures and shall document the inspection and any test
results to demonstrate proper installation. Interpretation:
Section 820.170 on installation requires that each
manufacturer establish and maintain adequate installation and inspection
instructions and, where appropriate, testing procedures. The purpose of this
requirement is to ensure that the device is properly installed and will
perform as intended after installation. This regulation applies to medical
device systems and complex devices that require set up and adjustment at the
location where they are to be used. For example, before a diagnostic x-ray
machine can be used, it has to be installed and adjusted and the performance
checked. Cardiopulmonary bypass machines also require set up and adjustment
at the user location. Manufacturers of such devices shall:
These instructions and procedures for proper
installation by the manufacturer's representative, user, or third party
(820.170) shall include instructions on how to determine that the installed
device is safe, performing satisfactorily and ready for use. Safety checks at
installation refer to safety aspects directly related to the installation and
setup activities and not to intrinsic safety features that have already been
checked during final acceptance testing at the factory. The instructions and procedures shall be
distributed with the device or otherwise made available to the person
installing the device. Such procedures and instructions are part of the
device master record and generally include a checklist for the installer to
make certain that all necessary installation and checkout activities have
been performed correctly. The installer should complete the checklist. If
available to the manufacturer, the filled-in checklist or other installation
records are part of the device history record. Installation and servicing are related activities. Therefore, see Chapter 16, Servicing, for more information.
|
|
|
|||
|
|
|
|
||||
|
Reference: www.FDA.gov The information provided here is for "public consumption" and is open to interpretation. MedicalDeviceSchool.com is not responsible for the content or the accuracy of the information. For all official interpretation and accuracy we ask that you consult the FDA's website directly and that you consult with your legal and regulatory experts on all matters of interpretation.. |
|
|
||||
|
|
|
|
|
|
|
|