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Annual Inspection
35
EN
12
Annual Inspection
Manufacturer’s specification
The manufacturer stipulates that qualified personnel or hospital technicians
must regularly test the device to assess its functionality and technical safety.
These inspections have to be carried out on an annual basis. Regular inspections
will assist in early detection of possible malfunctions. This helps preserve the de-
vice and increases its safety and service life.
Inspection tests
The tests described in this chapter are designed specifically for trained personnel
or a hospital technician. The operation of the device as well as its functionality
and serviceability are easily checked. Each test conducted has to be documented
with date and signature in chapter 19.1 "Test Log".
Measured values and tolerances
The following measuring tools and resources were used by the manufacturer to
determine the listed measurements and tolerances:
• Original cassette tubing
• Fluid bags
• Graduated measuring cup with 1.0 l scaling
• Stopwatch
WARNING!
If the specified parameters and tolerances are not met, an authorized service
technician must check the device.
12.1
Electrical Safety Test
1. Perform a visual inspection. Make sure that
• the fuse corresponds with the specifications indicated by the manufactur-
er,
• labels and stickers on device are legible,
• the mechanical condition of the device allows for its safe use,
• the device is clean to ensure proper and safe functionality.
2. Perform the measurement of the touch current (max. 100
μ
A in normal con-
dition and max. 500
μ
A in single fault condition) according to IEC 60601-1 /
EN 60601-1.
As an alternative, perform safety test according to IEC 62353.
12.2
Basic Function Test
A basic function test checks the displays, keys, and performance of the device. For
this test, you will need the following:
• the disposable cassette tube set
• a fluid bag (3 l)
• stopwatch
• one 1-liter measuring cup (100 ml scaling)
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: ......