SSH EN 301 839-2 V1.2.1:2007

Çështjet e pajtueshmërisë Elektromagnetike dhe të spektrit të Radios (ERM); Pajisje me Rreze të Shkurtër (SRD); Implantet Mjekësore Aktive me Fuqi Ultra të Ulët (ULP-AMI) dhe pajisjet Periferike (ULP-AMI-P) që punojnë në diapazonin e frekuencave nga 402 MHz deri në 405 MHz; Pjesa 2: EN i harmonizuar që mbulon kërkesat thelbësore të artikullit 3.2 të Direktivës R&TTE

Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Ultra Low Power Active Medical Implants (ULP-AMI) and Peripherals (ULP-AMI-P) operating in the frequency range 402 MHz to 405 MHz; Part 2: Harmonized EN covering essential requirements of article 3.2 of the R&TTE Directive

Scope

The present document applies to the following radio equipment types:
• Ultra Low Power Active Medical Implants (ULP-AMI);
• and Peripherals (ULP-AMI-P).
These radio equipment types are capable of operating in all or any part of the frequency bands given below.
Table 1: Ultra Low Power Active Medical Implants (ULP-AMI) and
Peripherals (ULP-AMI-P) service frequency bands
Ultra Low Power Active Medical Implants (ULP-AMI) and
Peripherals (ULP-AMI-P) service frequency bands
Transmit Ultra Low Power Active Medical Implants
(ULP-AMI) and Peripherals (ULP-AMI-P)
402 MHz to 405 MHz
Receive Ultra Low Power Active Medical Implants
(ULP-AMI) and Peripherals (ULP-AMI-P)
402 MHz to 405 MHz
The present document is intended to cover the provisions of Directive 1999/5/EC [1] (R&TTE Directive).
Article 3.2, which states that "….. radio equipment shall be so constructed that it effectively uses the spectrum allocated
to terrestrial/space radio communications and orbital resources so as to avoid harmful interference".
An AIMD is regulated under the AIMD Directive 90/385/EEC [2]: radio parts contained therein (referred to herein as
ULP-AMI and ULP-AMI-P for peripheral devices) are regulated under the Directive 1999/5/EC [1].
In addition to the present document, other ENs that specify technical requirements in respect of essential requirements
under other parts of Article 3 of the R&TTE Directive [1] may apply to equipment within the scope of the present
document.
NOTE: A list of such ENs is included on the web site http://www.newapproach.org.