Glossary Of Symbols - 3M Espe elipar Betriebsanleitung

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Inhaltsverzeichnis

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as an applied part. The use of other light guides may

result in a reduction or increase in the light intensity.

The product's warranty does not cover any damage

resulting from the use of third-party light guides.

7 . Condensation resulting from the device being trans-

ferred from a cold to a warm environment may be a

potential risk. Never begin operating the device until

it has reached the ambient temperature.

8. In order to avoid electric shock, do not introduce

any objects into the device with the exception of

replacement parts handled in accordance with the

Operating Instructions.

9. Use only genuine 3M ESPE parts when replacing

defective components as directed in these Operating

Instructions. The product's warranty does not cover

any damage resulting from the use of third-party

replacement parts.

10. Should you have any reason to suspect the safety

of the device to be compromised, the device must

be taken out of operation and labeled accordingly

to prevent third parties from inadvertently using

a possibly defective device. Safety may be

compromised, e.g., if the device malfunctions or

is noticeably damaged.

11. Keep solvents, flammable liquids, and sources of

intense heat away from the device as they may

damage the plastic housing of the device, the seals,

or the operating buttons.

12. Do not operate the device in the proximity of

flammable mixtures.

13. Do not allow any cleaning agents to enter the device

during cleaning as they could cause an electrical

short or a dangerous malfunction.

14. Only service centers authorized by 3M Deutschland

GmbH may open the device housing and repair the

device.

15. Elipar must not be used in patients, or by users, with

heart pacemaker implants who have been advised

to be cautious with regard to their exposure to small

electrical devices.

16. Do not use Elipar in patients with a history of photo-

biological reactions (including individuals with

urticaria solaris or erythropoietic protoporphyria) or

who are currently on photosensitizing medication

(including 8-methoxypsoralen or dimethylchloro -

tetracycline).

17. Individuals with a history of cataract surgery may be

particularly sensitive to the exposure to light and

should be discouraged from Elipar treatment unless

adequate safety measures such as the use of

protective goggles to remove blue light are under -

taken.

18. Individuals with a history of retinal disease should

seek advice from their ophthalmologist prior to

operating the device. In operating the Elipar device,

this group of individuals must take extreme care and

comply with any and all safety precautions (including

the use of suitable light-filtering safety goggles).

19. This device has been developed and tested in

accordance with the relevant EMC regulations and

standards. It is in conformity with legal require-

ments. Since various factors such as power supply,

wiring, and the ambient conditions at the place of

operation can affect the EMC properties of the

device, the possibility that, under unfavorable

conditions, there will be EMC disruptions cannot be

completely excluded. If you should notice problems

in the operation of this or other devices, move

the device to a different location. The EMC manu -

facturer's declaration and the recommended

separation distances between portable and mobile

RF communications equipment and the Elipar unit

are listed in the appendix.

20. Prior to each use of the device ensure that the

emitted light intensity is sufficient to safely

guarantee polymerization. Check the light guide and

the light guide mounting hole to make sure they are

clean. If necessary, the light guide mounting hole

and the light guide can be cleaned as described in

the section "Maintenance and Care" (see also the

section "Measurement of Light Intensity").