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Guidelines and manufacturer's statement - electromagnetic compatibility
EN
14.4
Guidelines and Manufacturer’s Statement – Electromagnetic
Emissions
The device FLOSTEADY Arthroscopy Pump is intended for use in the electromag-
netic environment specified below. The user/operator of the FLOSTEADY Arthros-
copy Pump should make sure the device is operated within such an environment.
Emitted interference
measurements
Compliance
Electromagnetic environment guide-
lines
HF emission according
to CISPR 11
Group 1
The device FLOSTEADY Arthroscopy
Pump uses HF energy solely for its
internal functions. Therefore, the
camera's HF emission is very low and
it is unlikely that devices in close
proximity will experience interfer-
ence.
HF emission according
to CISPR 11
Class B
The device FLOSTEADY Arthroscopy
Pump is suitable for use in all facili-
ties including those in residential
areas and those directly connected
to a public utility network supplying
buildings used for residential pur-
poses as well.
Emission of harmonic
oscillations according
to IEC 61000-3-2
Class A
Emission of voltage
fluctuations / flickers
according to IEC 61000-
3-3
In compliance
Содержание Flosteady Arthroscopy Pump 200
Страница 6: ......
Страница 8: ...EN 18 Warranty and Service 47 19 Appendix 49 19 1 Test Log 49 Index 50 ...
Страница 31: ...User Menu 25 EN User Menu Overview ...
Страница 55: ...Appendix 49 EN 19 Appendix 19 1 Test Log Date Results Comment Signature ...
Страница 58: ...DE 18 Garantie und Kundendienst 50 19 Anhang 52 19 1 Testprotokoll 52 Index 53 ...
Страница 83: ...Anwendermenü 27 DE Übersicht zum Anwendermenü ...
Страница 108: ...52 Anhang DE 19 Anhang 19 1 Testprotokoll Datum Ergebnis Bemerkung Unterschrift ...
Страница 110: ...54 Index DE V Vor der Operation 31 Vorsichtsmaßnahmen 13 W Wartungsintervall alle zwei Jahre 33 ...
Страница 112: ...FR 18 Garantie et assistance technique 49 19 Annexe 51 19 1 Procès verbal de tests 51 Index alphabétique 52 ...
Страница 137: ...Menu de l utilisateur 27 FR Plan d ensemble ...
Страница 161: ...Annexe 51 FR 19 Annexe 19 1 Procès verbal de tests Date Résultat Remarque Signature ...
Страница 163: ...Index alphabétique 53 FR U Utilisation clinique 7 V Valeurs de mesure et tolérances 37 ...
Страница 164: ......
Страница 166: ...NL 18 Garantie en Klantenservice 50 19 Bijlage 52 19 1 Testprotocol 52 Index 53 ...
Страница 191: ...Gebruikersmenu 27 NL Overzicht bij het gebruikersmenu ...
Страница 216: ...52 Bijlage NL 19 Bijlage 19 1 Testprotocol Datum Resultaat Opmerking Handtekening ...
Страница 218: ...54 Index NL Voorschrift van de fabrikant 33 38 Voorzorgsmaatregelen 13 ...
Страница 220: ...PL 18 Gwarancja i obsługa klientów 49 19 Aneks 51 19 1 Protokół testowy 51 Skorowidz 52 ...
Страница 245: ...Menu użytkownika 27 PL Przegląd menu użytkownika ...
Страница 269: ...Aneks 51 PL 19 Aneks 19 1 Protokół testowy Data Wynik Uwagi Podpis ...
Страница 271: ......