DS/EN 302 510 V2.1.1:2017

Kortdistance apparater (SRD); ultra lav energi aktive medicinske implantater (ULP-AMI-M) og eksterne enheder (ULP-AMI-P), der opererer i frekvensområdet 30 MHz til 37,5 MHz; Harmoniseret standard, der dækker de væsentlige krav i artikel 3, stk. 2 i Direktiv 2014/53/EU


Status:
Gældende
Type:
Standard
Sprog:
Engelsk
Pris fra:
kr. 145,00

Beskrivelse

The present document applies to Ultra Low Power-Active Medical Membrane Implants and Membrane Implant
Peripherals as described in Directive 90/385/EEC [i.4], covering all active medical implants, that operate in a Medical
Implant Communications System in the frequency band 30 MHz to 37,5 MHz.
Table 1: Ultra Low Power Active Medical Membrane Implants and
Peripherals operating in the frequency band 30 MHz to 37,5 MHz
Ultra Low Power Active Medical Membrane Implants
and Peripherals service frequency bands
Transmitters – Ultra Low Power Active Medical
Membrane Implants and peripherals 30 MHz to 37,5 MHz
Receivers – Ultra Low Power Active Medical
Membrane Implants and peripherals 30 MHz to 37,5 MHz
The present document contains the technical requirements for characteristics of ULP-AMI-M and ULP-AMI-M-P radio
equipment which are aligned with annex 12 Sub-band (d) of CEPT/ERC Recommendation 70-03 [i.6].
The frequency usage conditions for the band 30 MHz to 37,5 MHz are EU wide harmonised for the SRD category
"active medical implant devices" according to 2013/752/EU [i.10] with the following usage restrictions:
• "This set of usage conditions is only available to ultra-low power medical membrane implants for blood
pressure measurements within the definition of active implantable medical devices in Directive 90/385/EEC."
The present document contains requirements to demonstrate that Ultra Low Power Active Medical Membrane Implants
and peripherals used in a medical membrane implant communications system "… shall be so constructed that it both
effectively uses and supports the efficient use of radio spectrum in order to avoid harmful interference" (article 3.2 of
the Directive 2014/53/EU [i.1]). It does not necessarily include all the characteristics, which may be required by a user,
nor does it necessarily represent the optimum performance achievable.

Antal sider: 41

Udgivet: 2017-01-12

Godkendelsesdato: 2017-01-09

Internationale relationer : ETSI EN 302 510 V2.1.1 (2017-01) IDT

ICS: 11.040.40 - Implantater til kirurgi, protetik og ortoptik 33.060.20 - Modtage- og sendeudstyr

Varenummer: M311441


Udvalg og komiteer

Komite

  • ETSI/ERM/TG30
  • ETSI/TR & TS

Dansk udvalg

DS/V-002