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42
Guidelines and manufacturer's statement - electromagnetic compatibility
EN
14.6
Guidelines and Manufacturer's Statement - Electromagnetic In-
terference Immunity - for the Device FLOSTEADY Arthroscopy
Pump
Note 1: The higher frequency range applies for 80 and 800 MHz.
Note 2: These guidelines are probably not realizable in all cases. The distribution
and spread of electromagnetic quantities differs depending on the absorption
and reflection of buildings, objects, and people.
Electromagnetic
interference
immunity tests
Test level
Compliance
Electromagnetic environ-
ment guidelines
Conducted HF
interference
quantities
according to IEC
61000-4-6
Radiated HF
interference
quantities
according to IEC
61000-4-3
3 V
eff
150 kHz to
80 MHz
3 V/m
80 MHz to
2.5 GHz
In compliance
In compliance
Portable and mobile wire-
less devices should not be
used in closer proximity to
the device FLOSTEADY
Arthroscopy Pump (includ-
ing cables/lines) than the
recommended safety dis-
tance calculated based on
the transmitting frequency
and the applicable for-
mula. Recommended
safety distance:
d = 1.2
P for 150 KHz
to 80 MHz
d = 1.2
P for 80 MHz to
800 MHz
d = 2.3
P for 800 MHz
to 2.5 GHz
With
P
as the rated output
of the transmitter in watts
[W] according to the infor-
mation provided by the
manufacturer of the trans-
mitter and
d
as recom-
mended safety distance in
meters [m].
The field strength of sta-
tionary transmitters for all
frequencies tested on site
a
should be lower than the
concordance level.
b
Interference is possible in
the proximity of devices
featuring the following
pictograph.
Summary of Contents for Flosteady Arthroscopy Pump 200
Page 6: ......
Page 8: ...EN 18 Warranty and Service 47 19 Appendix 49 19 1 Test Log 49 Index 50 ...
Page 31: ...User Menu 25 EN User Menu Overview ...
Page 55: ...Appendix 49 EN 19 Appendix 19 1 Test Log Date Results Comment Signature ...
Page 58: ...DE 18 Garantie und Kundendienst 50 19 Anhang 52 19 1 Testprotokoll 52 Index 53 ...
Page 83: ...Anwendermenü 27 DE Übersicht zum Anwendermenü ...
Page 108: ...52 Anhang DE 19 Anhang 19 1 Testprotokoll Datum Ergebnis Bemerkung Unterschrift ...
Page 137: ...Menu de l utilisateur 27 FR Plan d ensemble ...
Page 161: ...Annexe 51 FR 19 Annexe 19 1 Procès verbal de tests Date Résultat Remarque Signature ...
Page 163: ...Index alphabétique 53 FR U Utilisation clinique 7 V Valeurs de mesure et tolérances 37 ...
Page 164: ......
Page 166: ...NL 18 Garantie en Klantenservice 50 19 Bijlage 52 19 1 Testprotocol 52 Index 53 ...
Page 191: ...Gebruikersmenu 27 NL Overzicht bij het gebruikersmenu ...
Page 216: ...52 Bijlage NL 19 Bijlage 19 1 Testprotocol Datum Resultaat Opmerking Handtekening ...
Page 218: ...54 Index NL Voorschrift van de fabrikant 33 38 Voorzorgsmaatregelen 13 ...
Page 220: ...PL 18 Gwarancja i obsługa klientów 49 19 Aneks 51 19 1 Protokół testowy 51 Skorowidz 52 ...
Page 245: ...Menu użytkownika 27 PL Przegląd menu użytkownika ...
Page 269: ...Aneks 51 PL 19 Aneks 19 1 Protokół testowy Data Wynik Uwagi Podpis ...
Page 271: ......