ETSI TR 102 315-2004 Electromagnetic compatibility and Radio spectrum Matters (ERM) Short Range Devices (SRD) Ultra Low Power Animal Implant Devices (ULP-AID) operating in the freq_1.pdf
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1、 ETSI TR 102 315 V1.2.1 (2004-11)Technical Report Electromagnetic compatibilityand Radio spectrum Matters (ERM);Short Range Devices (SRD);Ultra Low Power Animal Implant Devices (ULP-AID)operating in the frequency band: 12,5 MHz to 20 MHz;System Reference DocumentETSI ETSI TR 102 315 V1.2.1 (2004-11)
2、 2 Reference RTR/ERM-RM-040 Keywords SRDoc, radio, SRD, HF, MF ETSI 650 Route des Lucioles F-06921 Sophia Antipolis Cedex - FRANCE Tel.: +33 4 92 94 42 00 Fax: +33 4 93 65 47 16 Siret N 348 623 562 00017 - NAF 742 C Association but non lucratif enregistre la Sous-Prfecture de Grasse (06) N 7803/88 I
3、mportant notice Individual copies of the present document can be downloaded from: http:/www.etsi.org The present document may be made available in more than one electronic version or in print. In any case of existing or perceived difference in contents between such versions, the reference version is
4、 the Portable Document Format (PDF). In case of dispute, the reference shall be the printing on ETSI printers of the PDF version kept on a specific network drive within ETSI Secretariat. Users of the present document should be aware that the document may be subject to revision or change of status. I
5、nformation on the current status of this and other ETSI documents is available at http:/portal.etsi.org/tb/status/status.asp If you find errors in the present document, please send your comment to one of the following services: http:/portal.etsi.org/chaircor/ETSI_support.asp Copyright Notification N
6、o part may be reproduced except as authorized by written permission. The copyright and the foregoing restriction extend to reproduction in all media. European Telecommunications Standards Institute 2004. All rights reserved. DECTTM, PLUGTESTSTM and UMTSTM are Trade Marks of ETSI registered for the b
7、enefit of its Members. TIPHONTMand the TIPHON logo are Trade Marks currently being registered by ETSI for the benefit of its Members. 3GPPTM is a Trade Mark of ETSI registered for the benefit of its Members and of the 3GPP Organizational Partners. ETSI ETSI TR 102 315 V1.2.1 (2004-11) 3 Contents Int
8、ellectual Property Rights4 Foreword.4 1 Scope 5 2 References 5 3 Definitions, symbols and abbreviations .6 3.1 Definitions6 3.2 Symbols6 3.3 Abbreviations .6 4 Executive summary 6 4.1 Status of the System Reference Document.6 4.2 Technical issues7 4.2.1 System description7 4.2.2 Market briefing .7 4
9、.2.3 Spectrum requirement and justifications.7 4.2.4 Current regulations .7 4.2.5 Proposed regulation 7 4.2.6 Compatibility issues8 5 Main conclusions8 5.1 Expected timing for products to market .8 5.2 ECC and ETSI actions8 Annex A: Detailed market information .9 A.1 Range of applications .9 A.2 Mar
10、ket size and value.9 A.3 Traffic evaluation .9 Annex B: Technical information 10 B.1 Detailed technical description 10 B.1.1 Magnetic field requirements for inductive systems10 B.2 Technical justifications for spectrum .11 B.2.1 Maximum Field Strength Level11 B.2.2 Frequency.11 B.2.3 Bandwidth and o
11、ther radio parameters.11 B.3 Information on current version of relevant ETSI standard.11 Annex C: Expected compatibility issues 12 C.1 Coexistence studies 12 C.2 Current ITU allocations12 C.3 Sharing issues.14 History 15 ETSI ETSI TR 102 315 V1.2.1 (2004-11) 4 Intellectual Property Rights IPRs essen
12、tial or potentially essential to the present document may have been declared to ETSI. The information pertaining to these essential IPRs, if any, is publicly available for ETSI members and non-members, and can be found in ETSI SR 000 314: “Intellectual Property Rights (IPRs); Essential, or potential
13、ly Essential, IPRs notified to ETSI in respect of ETSI standards“, which is available from the ETSI Secretariat. Latest updates are available on the ETSI Web server (http:/webapp.etsi.org/IPR/home.asp). Pursuant to the ETSI IPR Policy, no investigation, including IPR searches, has been carried out b
14、y ETSI. No guarantee can be given as to the existence of other IPRs not referenced in ETSI SR 000 314 (or the updates on the ETSI Web server) which are, or may be, or may become, essential to the present document. Foreword This Technical Report (TR) has been produced by ETSI Technical Committee Elec
15、tromagnetic compatibility and Radio spectrum Matters (ERM). ETSI ETSI TR 102 315 V1.2.1 (2004-11) 5 1 Scope The present document applies to the radio sections of inductive loop ULP-AID systems to be used by the medical and pharmaceutical industries in medically related animal studies of the efficacy
16、 and safety of drug and surgical procedures. These devices are typically simplex short-range transmitters and receiver systems that will operate in the following band, 12,5 MHz to 20 MHz. This spectrum is required due to European Treaty Series legislation 4 and 5 that stipulates certain requirements
17、 for housing animals used for experimental and scientific research. These devices are expected to be license exempt on a non-interference non-protection basis. The present document includes necessary information to support the co-operation between ETSI and the Electronic Communications Committee (EC
18、C) of the European Conference of Post and Telecommunications Administrations (CEPT), including: Detailed market information (annex A); Technical information (annex B); Expected compatibility issues (annex C). 2 References For the purposes of this Technical Report (TR) the following references apply:
19、 1 ETSI EN 302 195-1 (V1.1.1): “Electromagnetic compatibility and Radio spectrum Matters (ERM); Radio equipment in the frequency range 9 kHz to 315 kHz for Ultra Low Power Active Medical Implants (ULP-AMI) and accessories; Part 1: Technical characteristics and test methods“. 2 ETSI EN 302 195-2 (V1.
20、1.1): “Electromagnetic compatibility and Radio spectrum Matters (ERM); Radio equipment in the frequency range 9 kHz to 315 kHz for Ultra Low Power Active Medical Implants (ULP-AMI) and accessories; Part 2: Harmonized EN covering essential requirements of article 3.2 of the R b) the function they per
21、form in providing physiological data cannot reasonably be obtained by any other method; c) they are expected to reliably transmit data continuously with a duty cycle of 10 % or less in performing their intended function for periods of time on average of a month; d) they are capable of being refurbis
22、hed and reused at the end of their life cycle; e) they are not capable of being programmed by a programming device. The ambient noise level: The ambient noise is dependent on the location of the equipment. Medical facilities can be considered an industrial or commercial environment. In these environ
23、ments the ambient noise is very high. The main noise sources are the harmonics of different electric equipment, for example switch mode power supplies, personal computers, other medical equipment, ISM devices, fluorescent lights, electric distribution in general, etc. According to CEPT/ERC Report 44
24、 6, the noise level in this type of environment, measured in a 1 kHz bandwidth, is expected to vary in the range 5 dBA/m to 30 dBA/m at 50 kHz. A typical level is 13 dBA/m at 50 kHz. The noise level falls at a 3,5 dB/octave, and it is typically -1 dBA/m at 1 MHz. At 20 MHz the noise floor will be ap
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