ETSI EN 302 510-1 V1.1.1 (2007-07)

Intellectual Property Rights
Foreword
1 Scope
2 References
3 Definitions, symbols and abbreviations
  3.1 Definitions
  3.2 Symbols
  3.3 Abbreviations
4 Technical requirements & specifications
  4.1 General requirements
  4.2 Presentation of equipment for testing purposes
  4.3 Mechanical and electrical design
  4.4 Auxiliary test equipment
  4.5 Interpretation of the measurement results
5 Test conditions, power sources and ambient temperatures
  5.1 Normal and extreme test conditions
  5.2 Test power source
  5.3 Normal test conditions
  5.4 Extreme test conditions
6 General conditions
  6.1 Normal test signals and test modulation
  6.2 Antenna
  6.3 Test fixture
  6.4 Test sites and general arrangements for radiated measurements
  6.5 Modes of operation of the transmitter
  6.6 Measuring receiver
7 Transmitter requirements
  7.1 Transmitter definitions
  7.2 Maximum effective radiated power
  7.3 Out of Band Emissions
  7.4 Unwanted Emissions in the spurious domain
  7.5 Duty cycle
8 Receiver requirement
  8.1 Blocking or desensitization
  8.2 Receiver spurious radiation
9 Measurement uncertainty
Annex A (normative): Radiated measurement
    A.1 Test sites and general arrangements for measurements
        involving the use of radiated fields
    A.2 Guidance on the use of radiation test sites
    A.3 Standard test position
Annex B (normative): Technical performance of the spectrum analyser
Annex C (informative): Bibliography
History

Pertains to Ultra Low Power Active Medical membrane implant transmitters and receiver/activators operating in the range from 30 MHz to 37,5 MHz and any associated radio apparatus including patient related telecommunication devices using digital modulation techniques.