ETSI - EN 301 839-2
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
inactive
| Organization: | ETSI |
| Publication Date: | 1 April 2007 |
| Status: | inactive |
| Page Count: | 18 |
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.
Document History
October 1, 2009
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
A description is not available for this item.
July 1, 2009
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
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...
January 1, 2009
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
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...
July 1, 2007
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
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...
July 1, 2007
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
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...
EN 301 839-2
April 1, 2007
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
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...
May 1, 2006
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
The present document applies to Ultra Low Power-Active Medical Implants (ULP-AMI) and accessories as described in Directive 90/385/EEC [2], operating in a Medical Implant Communications System (MICS)...
June 1, 2002
Electromagnetic Compatibility and Radio Spectrum Matters (ERM); Radio Equipment in the Frequency Range 402 MHz to 405 MHz for Ultra Low Power Active Medical Implants and Accessories; Part 2: Harmonized EN Covering Essential Requirements of Article 3.2 of the R&TTE Directive
Foreword
This Candidate Harmonized European Standard (Telecommunications series) has been produced by ETSI Technical Committee Electromagnetic compatibility and Radio spectrum Matters (ERM).
The...
April 1, 2002
Electromagnetic Compatibility and Radio Spectrum Matters (ERM); Radio Equipment in the Frequency Range 402 MHz to 405 MHz for Ultra Low Power Active Medical Implants and Accessories; Part 2: Harmonized EN Covering Essential Requirements of Article 3.2 of the R&TTE Directive
The present document applies to Ultra Low Power-Active Medical Implants (ULP-AMI) and accessories as described in Directive 90/385/EEC [4], operating in a Medical Implant Communications System (MICS)...
July 1, 2001
Electromagnetic Compatibility and Radio Spectrum Matters (ERM); Radio Equipment in the Frequency Range 402 MHz to 405 MHz for Ultra Low Power Active Medical Implants and Accessories; Part 2: Harmonized EN Covering Essential Requirements of Article 3.2 of the R&TTE Directive
The present document applies to Ultra Low Power-Active Medical Implants (ULP-AMI) and accessories as described in Directive 90/385/EEC [4], operating in a Medical Implant Communications System (MICS)...
December 1, 2000
Electromagnetic Compatibility and Radio Spectrum Matters (ERM); Radio Equipment in the Frequency Range 402 MHz to 405 MHz for Ultra Low Power Active Medical Implants and Accessories; Part 2: Harmonized EN Covering Essential Requirements of Article 3.2 of the R&TTE Directive
The present document applies to Ultra Low Power-Active Medical Implants (ULP-AMI) and accessories as described in Directive 90/385/EEC [4], operating in a Medical Implant Communications Service...