ﺍﻟﺩﻟﻳﻝ ﺍﻹﺭﺷﺎﺩﻱ ﻭﺑﻳﺎﻥ ﺍﻟﺷﺭﻛﺔ ﺍﻟ ﻣ ُ ﺻ ﻧ ﱢ ﻌﺔ - ﺍﻻﻧﺑﻌﺎﺛﺎﺕ ﺍﻟﻛﻬﺭﻭﻣﻐﻧﺎﻁﻳﺳﻳﺔ
.ﻫﺫﺍ ﻣ ُﻌﺩ ﻟﻼﺳﺗﺧﺩﺍﻡ ﻓﻲ ﺍﻟﺑﻳﺋﺔ ﺍﻟﻛﻬﺭﻭﻣﻐﻧﺎﻁﻳﺳﻳﺔ ﺍﻟﻣﺣﺩﺩﺓ ﺃﺩﻧﺎﻩ
.ﻋﻠﻰ ﺍﺳﺗﺧﺩﺍﻣﻪ ﻓﻲ ﻫﺫﻩ ﺍﻟﺑﻳﺋﺔ
ﻳﺟﺏ ﺃﻥ ﻳﺣﺭﺹ ﺍﻟﻌﻣﻳﻝ ﺃﻭ ﻣﺳﺗﺧﺩﻡ ﺍﻟﺟﻬﺎﺯ ﺍﻟﻁﺑﻲ ﺍﻟﻛﻬﺭﺑﺎﺋﻲ
IRT 6520/6020
ﺍﻟﺑﻳﺋﺔ ﺍﻟﻛﻬﺭﻭﻣﻐﻧﺎﻁﻳﺳﻳﺔ - ﺍﻟﺩﻟﻳﻝ ﺍﻹﺭﺷﺎﺩﻱ
ﻳﺳﺗﺧﺩﻡ ﻫﺫﺍ ﺍﻟﺟﻬﺎﺯ ﺍﻟﻁﺑﻲ ﺍﻟﻛﻬﺭﺑﺎﺋﻲ ﻁﺎﻗﺔ ﺫﺍﺕ ﺗﺭﺩﺩ ﺭﺍﺩﻳﻭﻱ ﻷﺩﺍء
ﻭﻅﻳﻔﺗﻪ ﺍﻟﺩﺍﺧﻠﻳﺔ ﻓﻘﻁ. ﻭﻣﻥ ﺛﻡ ﻓﺈﻥ ﺍﻻﻧﺑﻌﺎﺛﺎﺕ ﺫﺍﺕ ﺍﻟﺗﺭﺩﺩ ﺍﻟﺭﺍﺩﻳﻭﻱ
ﺍﻟﻣﻧﻁﻠﻘﺔ ﻣﻧﻪ ﺗﻛﻭﻥ ﻗﻠﻳﻠﺔ ﺟ ﺩ ً ﺍ ﻭﻻ ﻳﺭﺟﺢ ﺃﻥ ﺗﺳﺑﺏ ﺃﻱ ﺗﺩﺍﺧﻝ ﻣﻊ ﺃﻱ ﺟﻬﺎﺯ
.ﺇﻟﻛﺗﺭﻭﻧﻲ ﻗﺭﻳﺏ
ﻣﺗﻭﺍﻓﻕ
.ﻳﻌﺗﻣﺩ ﻫﺫﺍ ﺍﻟﺟﻬﺎﺯ ﺍﻟﻁﺑﻲ ﺍﻟﻛﻬﺭﺑﺎﺋﻲ ﻋﻠﻰ ﺍﻟﺑﻁﺎﺭﻳﺎﺕ ﻓﻘﻁ ﻛﻣﺻﺩﺭ ﻟﻠﻁﺎﻗﺔ
ﺣﺳﺎﺏ ﺍﻟﻣﺳﺎﻓﺔ ﺍﻟﻔﺎﺻﻠﺔ ﻟﻸﺟﻬﺯﺓ ﻏﻳﺭ ﺍﻟﺩﺍﻋﻣﺔ ﻟﻠﺣﻳﺎﺓ
(ﻓﻭﻟﺕ/ﻣﺗﺭ
/ ﻓﻭﻟﺕ ﺟﺫﺭ ﻣﺗﻭﺳﻁ ﻣﺭﺑﻊ
3
(ﺍﻟﻣﺳﺎﻓﺔ ﺍﻟﻔﺎﺻﻠﺔ ﻭﻓ ﻘ ً ﺎ ﻟﺗﺭﺩﺩ ﺟﻬﺎﺯ ﺍﻹﺭﺳﺎﻝ )ﺑﺎﻟﻣﺗﺭ
ﺟﻳﺟﺎ ﻫﺭﺗﺯ
ﻣﻳﺟﺎ ﻫﺭﺗﺯ ﺇﻟﻰ
ﻣﻳﺟﺎ ﻫﺭﺗﺯ
2,5
800
80
ﻣﻳﺟﺎ
ﺇﻟﻰ
800
ﻫﺭﺗﺯ
7
3,5
d = [
] P
d = [
] P
E
E
1
1
0,23
0,12
0,74
0,37
2,33
1,17
7,38
3,69
23,33
11,67
92
ﺍﻟﺟﻬﺎﺯ ﺍﻟﻁﺑﻲ ﺍﻟﻛﻬﺭﺑﺎﺋﻲ
IRT 6520/6020
ﺍﻟﺗﻭﺍﻓﻕ
ﺍﺧﺗﺑﺎﺭ ﺍﻻﻧﺑﻌﺎﺛﺎﺕ
ﺍﻻﻧﺑﻌﺎﺛﺎﺕ ﺫﺍﺕ ﺍﻟﺗﺭﺩﺩ
ﺍﻟﻣﺟﻣﻭﻋﺔ
1
،ﺍﻟﺭﺍﺩﻳﻭﻱ
CISPR 11
ﺍﻻﻧﺑﻌﺎﺛﺎﺕ ﺫﺍﺕ ﺍﻟﺗﺭﺩﺩ
ﺍﻟﻔﺋﺔ ﺏ
،ﺍﻟﺭﺍﺩﻳﻭﻱ
CISPR 11
ﺍﻻﻧﺑﻌﺎﺛﺎﺕ ﺍﻟﻣﺗﺟﺎﻧﺳﺔ
ﻻ ﻳﻧﻁﺑﻕ
IEC 61000-3-2
ﺗﻘﻠﺑﺎﺕ ﺍﻟﺟﻬﺩ/ﺍﻻﻧﺑﻌﺎﺛﺎﺕ
ﻻ ﻳﻧﻁﺑﻕ
ﺍﻟﻭﺍﻣﺿﺔ
)ﺗﻭﺍﻓﻕ
3
ﻛﻳﻠﻭ ﻫﺭﺗﺯ ﺇﻟﻰ
80
150
ﺃﻗﺻﻰ ﺗﻘﺩﻳﺭ ﻟﻠﻁﺎﻗﺔ ﺍﻟﺧﺎﺭﺟﺔ
ﻣﻳﺟﺎ ﻫﺭﺗﺯ ﻓﻲ
(ﻣﻥ ﺟﻬﺎﺯ ﺍﻹﺭﺳﺎﻝ )ﺑﺎﻟﻭﺍﺕ
ﺍﻟﻧﻁﺎﻗﺎﺕ ﺍﻟﻼﺳﻠﻛﻳﺔ
ﺍﻟﺻﻧﺎﻋﻳﺔ ﻭﺍﻟﻌﻠﻣﻳﺔ
(
) ﻭﺍﻟﻁﺑﻳﺔ
ISM
3,5
d = [
] P
V
1
0,12
0,01
0,37
0,1
1,17
1
3,69
10
11,67
100
(ﺩﺭﺟﺔ ﻓﻬﺭﻧﻬﺎﻳﺕ
ﺩﺭﺟﺔ ﻣﺋﻭﻳﺔ
108-93,2)
(ﺩﺭﺟﺔ ﻓﻬﺭﻧﻬﺎﻳﺕ
ﺩﺭﺟﺔ ﻣﺋﻭﻳﺔ
104-50)
()-31–131 ﺩﺭﺟﺔ ﻓﻬﺭﻧﻬﺎﻳﺕ
-52–55 ﺩﺭﺟﺔ ﻣﺋﻭﻳﺔ
(ﺭﻁﻭﺑﺔ ﻧﺳﺑﻳﺔ 01-59% )ﺩﻭﻥ ﺗﻛﺛﻳﻑ
ﺩﺭﺟﺔ ﻣﺋﻭﻳﺔ ﺃﻭ ﻓﻬﺭﻧﻬﺎﻳﺕ
ﺍﻟﺣﺩ ﺍﻷﻗﺻﻰ ﻟﻠﺧﻁﺄ ﺍﻟﻣﺧﺑﺭﻱ
(ﺩﺭﺟﺔ ﻓﻬﺭﻧﻬﺎﻳﺕ
ﺩﺭﺟﺔ ﻣﺋﻭﻳﺔ
0,4 ±)
(ﺩﺭﺟﺔ ﻓﻬﺭﻧﻬﺎﻳﺕ
ﺩﺭﺟﺔ ﻣﺋﻭﻳﺔ
0,5 ±)
(ﺩﺭﺟﺔ ﻓﻬﺭﻧﻬﺎﻳﺕ
ﺩﺭﺟﺔ ﻣﺋﻭﻳﺔ
0,26 ±)
ﻗﻳﺎﺱ
ﺿﻐﻁ ﺟﻭﻱ
ﺿﻐﻁ ﺟﻭﻱ ﺃﻭ ﻋﻧﺩ ﺍﺭﺗﻔﺎﻋﺎﺕ ﺫﺍﺕ ﺿﻐﻁ ﺟﻭﻱ ﻳﺻﻝ ﺇﻟﻰ
1
ﺃﺑﻘﻪ ﺟﺎ ﻓ ً ﺎ
ﺩﺭﺟﺔ ﺣﺭﺍﺭﺓ ﺍﻟﺗﺧﺯﻳﻥ
Standard Reference Edition Title:
EN 12470-5: 2003 Clinical thermometers – Part 5: Performance of infra-red ear thermometers (with
maximum device).
EN 60601-1: 2006 Medical electrical equipment – Part 1: General requirements for basic safety and essential
performance.
EN ISO 14971: 2014 Medical devices – Application of risk management to medical devices.
EN ISO 10993-1: 2009 Biological evaluation of medical devices – Part 1: Evaluation and testing within a risk
management process.
EN 60601-1-2: 2007 Medical electrical equipment – Part 1-2: General requirements for basic safety and
essential performance – Collateral standard: Electromagnetic compatibility – Requirements and tests.
EN 980: 2008 Symbols for use in labeling of medical devices.
EN 1041: 2008 Information supplied by the manufacturer of medical devices.
EN 60601-1-11: 2010 Medical electrical equipment – Part 1-11: General requirements for basic safety and
essential performance -- Collateral standard: Requirements for medical electrical equipment and medical
electrical systems used in the home healthcare environment.
ﺍﻷﺟﻬﺯﺓ ﺍﻟﻁﺑﻳﺔ ﺍﻟﻛﻬﺭﺑﺎﺋﻳﺔ ﺗﺣﺗﺎﺝ ﺇﻟﻰ ﺗﺩﺍﺑﻳﺭ ﻭﻗﺎﺋﻳﺔ ﺧﺎﺻﺔ ﻓﻳﻣﺎ ﻳﺗﻌﻠﻕ ﺑﺎﻟﺗﻭﺍﻓﻕ ﺍﻟﻛﻬﺭﻭﻣﻐﻧﺎﻁﻳﺳﻲ. ﻟﻭﺻﻑ ﺗﻔﺻﻳﻠﻲ ﻟﻣﺗﻁﻠﺑﺎﺕ
.(( ﺗﻔﺿﻝ ﺑﺎﻻﺗﺻﺎﻝ ﺑﻣﺭﻛﺯ ﺍﻟﺧﺩﻣﺔ ﺍﻟﻣﺣﻠﻲ ﺍﻟﻣﻌﺗﻣﺩ ﺍﻟﺧﺎﺹ ﺑﻙ )ﺍﻧﻅﺭ ﺑﻁﺎﻗﺔ ﺍﻟﺿﻣﺎﻥ
.ﻳﻣﻛﻥ ﻷﺟﻬﺯﺓ ﺍﻻﺗﺻﺎﻝ ﺍﻟﻣﺣﻣﻭﻟﺔ ﻭﺃﺟﻬﺯﺓ ﺍﻻﺗﺻﺎﻝ ﺍﻟﻣﺗﻧﻘﻠﺔ ﺫﺍﺕ ﺍﻟﺗﺭﺩﺩ ﺍﻟﺭﺍﺩﻳﻭﻱ ﺃﻥ ﺗﺅﺛﺭ ﻋﻠﻰ ﺍﻷﺟﻬﺯﺓ ﺍﻟﻁﺑﻳﺔ ﺍﻟﻛﻬﺭﺑﻳﺔ
.ﻳﺭﺟﻰ ﻋﺩﻡ ﺍﻟﺗﺧﻠﺹ ﻣﻥ ﺍﻟﻣﻧﺗﺞ ﻓﻲ ﺍﻟﻧﻔﺎﻳﺎﺕ ﺍﻟﻣﻧﺯﻟﻳﺔ ﻓﻲ ﻧﻬﺎﻳﺔ ﻋﻣﺭ ﺍﺳﺗﺧﺩﺍﻣﻪ
.ﻟﺣﻣﺎﻳﺔ ﺍﻟﺑﻳﺋﺔ، ﺗﺧﻠﺹ ﻣﻥ ﺍﻟﺑﻁﺎﺭﻳﺎﺕ ﺍﻟﻔﺎﺭﻏﺔ ﻓﻲ ﻣﻭﺍﻗﻊ ﺍﻟﺟﻣﻊ ﺍﻟﻣﻼﺋﻣﺔ ﻁﺑ ﻘ ً ﺎ ﻟﻠﻭﺍﺋﺢ ﺍﻟﻭﻁﻧﻳﺔ ﺃﻭ ﺍﻟﻣﺣﻠﻳﺔ
ﻣﻭﺍﺻﻔﺎﺕ ﺍﻟﻣﻧﺗﺞ
:ﻧﻁﺎﻕ ﺩﺭﺟﺔ ﺍﻟﺣﺭﺍﺭﺓ ﺍﻟﻣﻌﺭﻭﺿﺔ
42,2-34
:ﻧﻁﺎﻕ ﺩﺭﺟﺔ ﺣﺭﺍﺭﺓ ﻣﺣﻳﻁ ﺍﻟﺗﺷﻐﻳﻝ
40-10
:ﻧﻁﺎﻕ ﺩﺭﺟﺔ ﺣﺭﺍﺭﺓ ﺍﻟﺗﺧﺯﻳﻥ
:ﺍﻟﺭﻁﻭﺑﺔ ﺍﻟﻧﺳﺑﻳﺔ ﻟﻠﺗﺷﻐﻳﻝ ﻭﺍﻟﺗﺧﺯﻳﻥ
:ﺩﻗﺔ ﺍﻟﻌﺭﺽ
0.1
ﺩﻗﺔ ﻧﻁﺎﻕ ﺩﺭﺟﺔ ﺍﻟﺣﺭﺍﺭﺓ ﺍﻟﻣﻌﺭﻭﺿﺔ
ﺩﺭﺟﺔ ﻣﺋﻭﻳﺔ
ﺩﺭﺟﺔ ﻣﺋﻭﻳﺔ
42-
:(ﺩﺭﺟﺔ ﻓﻬﺭﻧﻬﺎﻳﺕ
ﺩﺭﺟﺔ ﻓﻬﺭﻧﻬﺎﻳﺕ
0,2 ±
107,6-
:ﺧﺎﺭﺝ ﻫﺫﺍ ﺍﻟﻧﻁﺎﻕ
0,3 ±
:ﺍﻟﺗﺭﺩﺩ ﺍﻹﻛﻠﻳﻧﻳﻛﻲ
0,14 ±
ﻋﺎﻣﺎﻥ
:ﻋﻣﺭ ﺍﻟﺑﻁﺎﺭﻳﺔ
600/
ﺳﻧﻭﺍﺕ
:ﻋﻣﺭ ﺍﻟﺧﺩﻣﺔ
5
ﻣﻘﻳﺎﺱ ﺍﻟﺣﺭﺍﺭﺓ ﻫﺫﺍ ﻣﺧﺻﺹ ﻟﻠﻌﻣﻝ ﻋﻧﺩ
1
ﻫﻛﺗﻭ ﺑﺎﺳﻛﺎﻝ
.(
1060 – 700)
40 °C
10 °C
ﺩﺭﺟﺔ ﺣﺭﺍﺭﺓ ﺍﻟﺗﺷﻐﻳﻝ
ﺍﻟﺟﻬﺎﺯ ﻣﻊ ﻗﻁﻊ ﻣﻁﺑﻘﺔ ﺍﻧﻅﺭ ﺗﻌﻠﻳﻣﺎﺕ ﺍﻻﺳﺗﺧﺩﺍﻡ
ﻣﻥ ﺍﻟﻧﻭﻉ
BF
.ﻋﺭﺿﺔ ﻟﻠﺗﻐﻳﻳﺭ ﺩﻭﻥ ﺇﺷﻌﺎﺭ
:ﻳﻣﺗﺛﻝ ﻫﺫﺍ ﺍﻟﺟﻬﺎﺯ ﻟﻠﻣﻌﺎﻳﻳﺭ ﺍﻟﺗﺎﻟﻳﺔ
ﻳﻣﺗﺛﻝ ﻫﺫﺍ ﺍﻟﻣﻧﺗﺞ ﻟﺷﺭﻭﻁ ﻭﺛﻳﻘﺔ ﺍﻟﻠﺟﻧﺔ ﺍﻷﻭﺭﻭﺑﻳﺔ
) ﺍﻟﺗﻭﺍﻓﻕ ﺍﻟﻛﻬﺭﻭﻣﻐﻧﺎﻁﻳﺳﻲ
EMC
35
)
95
93