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INSTRUCTIONS FOR USE SUPPORTS AND STANDS

5

  INSPECTION AND MAINTENANCE

Medical products shall be subject to regular maintenance and inspection cycles. This is essential for compliance 
with safety requirements. The manufacturer of the medical device is responsible for the defi nition of regular mea-
sures to ensure this. The operator is responsible for the implementation of defi ned measures

5.1  RECURRING INSPECTIONS AND MAINTENANCE

INSPECTION AND MAINTENANCE

Use disinfected areas only when the disinfectant has dried!

Use disinfected areas only after the disinfectant is dry!

Do not sterilise! If sterilisation should be mandatory (e.g. administrative requirement), make sure to consult 
the manufacturer.

WARNING – HEALTH HAZARD

Disinfectants may contain hazardous substances which may cause injuries after contact with skin or 
eyes, or may damage the respiratory system when inhaled. Observe the measures for protection:

Follow the instructions of the disinfectant manufacturer!

Observe the hygiene guidelines!

For all maintenance and audit work, switch the light to stand-by and unplug and disconnect the 
light from the mains. Secure the light against reconnection.

WARNING – DANGER OF INJURY
The support arm is spring loaded and can snap up during the removal of the light head – danger of injury!

NOTE – INSPECTIONS
The operator shall check and service all support systems for the following points:

DIN EN 62353 is to be observed for the periodic inspections (see “Inspection schedule” in the annex).

Every six months:

Deformation of the support system

Cracks in the plastic parts

Paint damages

Annually:

Extended check of the support system such as e.g. holding force of the spring arm, Check mounting bolt 
at the bottom of mobile stand foot and tighten, if necessary.

Extended functional check, such as free movement of the joints 

Inspect and lubricate locking segment as in Section „Lubricate locking segment“ of the instructions for 
use of the holding systems.

Electric safety inspection

In the event of any faults or damage, please contact your supplier.

Your supplier has been informed and trained regarding the scope and contents of the maintenance work.

For the inspection and maintenance work of the light head please observe the Instructions for Use for 

“Minor surgical lights 

MIMLED 600 

 and 

MIMLED 1000 

“.

Summary of Contents for MIMLED 1000

Page 1: ...INSTRUCTIONS FOR USE SUPPORTS AND STANDS FOR MIMLED 600 MIMLED 1000 VALID FROM MAY 2016...

Page 2: ...2 INSTRUCTIONS FOR USE SUPPORTS AND STANDS...

Page 3: ...ECTION 9 4 1 General safety instructions 4 2 Cleaning 4 3 Disinfection 9 9 9 5 INSPECTION AND MAINTENANCE 10 5 1 Periodical testing and maintenance 10 6 MAINTENANCE 11 6 1 Setting the spring force 6 2...

Page 4: ...TIONS FOR USE Please read these Instructions for Use carefully before you firstusethesupportsystem This will allow you to get all of the advantages which the support system offers and avoid possible i...

Page 5: ...e light body 2 4 CONTRAINDICATION The support arm system should not be located in the vicinity of strong magnetic fields Only lights of type MIMLED 600 and MIMLED 1000 may be con nected to the support...

Page 6: ...EALTH HAZARD Disinfectants can contain harmful substances which in contact with skin and eyes may cause injury or damage to the respiratory system through inhalation Adhere to protective measures Obse...

Page 7: ...C SHOCK To avoid risk of electric shock the device may only be connected to supply mains with a protective earth conductor The device must be connected so that it can be completely all poles and at th...

Page 8: ...isposal For proper disposal of the system please contact an authorised disposal business You can obtain their address from your environmental officer or at your local municipality NOTE Do not dispose...

Page 9: ...en is recommended Surfaces to be disinfected every working day After the contamination with potentially infectious material e g blood secretions or excrement areas are to be immediately and specifical...

Page 10: ...ch the light to stand by and unplug and disconnect the light from the mains Secure the light against reconnection WARNING DANGER OF INJURY The support arm is spring loaded and can snap up during the r...

Page 11: ...djust spring force so that the spring arm with the end device remains in any desired position CAUTION DESTRUCTION OF THE SPRING ARM The adjusting of the spring force is done in the upper end position...

Page 12: ...king force control If the spring arm lowers the spring force is too low The adjusting screw must be rotated to the left counter clockwise If the spring arm rises the spring force is too high The adjus...

Page 13: ...end device according to Section Lubricate end device Locking segment 7 DISMANTLING AND REASSEMBLY FOR SERVICING 7 1 DISMANTLE END DEVICE NOTE QUALIFICATION OF PERSONNEL The dismantling reassembly mus...

Page 14: ...e 180 so that the locking segment is visible 4 Remove locking segment with a small screwdriver while holding the terminal firmly 5 Remove terminal from the support while holding the spring arm firmly...

Page 15: ...spring arm opening WARNING DANGER OF INJURY The spring arm which is pressed downwards can snap back up and cause injury During the installation of the end device no people should be located within th...

Page 16: ...r busbar in addition to the protective measures according to DIN VDE 0100 Part 410 This means protective bonding conductors must be connected to a potential equalizing busbar In particular when using...

Page 17: ...delivered B Ceiling mount bracket 1 Loosen the three threaded screws with a screwdriver 2 Pull canopy down 3 Remove and replace defective fuse 4 Insert new fuse 5 Pull canopy back upwards and tighten...

Page 18: ...rtable and mobile HF communication equipment may affect medical electrical devices The use of stands and mounting systems that do not come from deliveries as well as their components such as spring ar...

Page 19: ...ETWORK which supplies buildings used for residential purposes Aussendungen von Spannungsschwankungen nach IEC 61000 3 3 Complies GUIDELINES AND MANUFACTURER S DECLARATION ELECTROMAGNETIC IMMUNITY MIML...

Page 20: ...ables ac cording to EN 61000 4 6 150kHz 80MHz 3Vrms 150kHz 80MHz 10Vrms GUIDELINES AND MANUFACTURER S DECLARATION ELECTROMAGNETIC IMMUNITY Voltage dips short interrup tions an voltage variations on po...

Page 21: ...S BETWEEN PORTABLE AND MOBILE RF TELECOMMUNICATION EQUIPMENT AND THE DEVICE NOT LIFE SUPPORTING THE RECOMMENDED SEPARATION DISTANCES BETWEEN PORTABLE AND MOBILE RF TELE COMMUNICATION DEVICES AND MIMLE...

Page 22: ...ok O n o O ok O n o O ok O n o O ok O n o O ok O n o O ok O n o O ok O n o O ok O n o O ok O n o O The parts of the support system are not deformed The system is free of paint damage The plastic parts...

Page 23: ...__________ Signature stamp __________________ Date __________________________________________ Signature stamp 5th year 10th year __________________ Date ___________________________________________ Sig...

Page 24: ...MIMSAL TRADE S L C Mollet 17 Pol Ind Palou Nord 08401 GRANOLLERS Barcelona Telf 34 930 139 860 mimsal mimsal com www mimsal com...

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