F1SCHEDULE 2ATesting before arrival in Scotland

Annotations:
Amendments (Textual)

3

In this schedule,

  • “device” means an in vitro diagnostic medical device within the meaning given in regulation 2(1) of the Medical Devices Regulations 2002,

  • “sensitivity”, in relation to a device, means how often the device correctly generates a positive result, and

  • “specificity”, in relation to a device, means how often the device correctly generates a negative result.