active medical device definition

active medical device means any medical device relying for its functioning on a source of electrical energy or any source of power other than that directly generated by the human body or gravity;
active medical device means a medical device, the operation of which depends on a source of electrical energy or any other source of energy other than the energy generated by human or animal body or gravity;
active medical device means any medical device as defined in First Schedule of Medical Device Regulations 2012;

More Definitions of active medical device

active medical device means any medical device —
active medical device means a device whose operation depends on a source of electrical energy or any source of power other than that directly generated by the human body or gravity and which acts by converting this energy. Medical devices intended to transmit energy, substances or other elements between an active medical device and the patient, without any significant change, is not considered to be active medical devices.
active medical device means any medical device the operation of which depends on a source of electrical energy or any source of power other than that directly generated by the human body or gravity;
active medical device means any medical device of which the operation depends on a source of electrical energy or any source of power other than that directly generated by the human body or gravity and which acts by converting this to energy but excluding medical devices intended to transmit energy, substances or other elements between an active medical device and the user, without any significant change in the energy, substance or other element being transmitted;
active medical device means any medical device operation of which depends on a source of electrical energy or any source of power other than that directly generated
active medical device means any medical device as defined in First Schedule of

Related to active medical device

  • GCP means the Good Clinical Practices officially published by EMA, FDA and the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) that may be in effect from time to time and are applicable to the testing of the Compounds.