Bon E-20 Instruction manual

Instruction manual

bon E-20 SE

GA bon E-20 SE Rev 1.1 E 260406

PO Box 32 26	Phone: 0451/		80 900-0	Sparkasse zu Lübeck	Commerzbank Lübeck
23581 Lübeck	Fax:	0451/	80 900-10	(Sort code 230 501 01) Acc.No. 1 014 885	(Sort code 230 400 22)	Acc.No. 0 107 755
Stellmacherstraße 14	E-Mail:	[e-mail]		Swift / BIC: HSHN DE H1 SPL	Postbank Hamburg
D-23556 Lübeck	Internet: www.bon.de			IBAN: DE 2305 0101 0001 0148 85	(Sort code 200 100 20)	Acc.No. 409 22-204

bon Optic Vertriebsgesellschaft mbH – managing director: H. Jochen Kaber – HR Lübeck, HRB 3475 – VAT No. 161662634

DS

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Contents

1	Introduction .....................................................................................................			4
2	Important information.....................................................................................			5
	2.1	Information about the device ..............................................................................		5
	2.2	Intended purpose and classification ...................................................................		5
	2.3	Liability ...............................................................................................................		5
	2.4	Scope of delivery................................................................................................		6
3	Safety instructions..........................................................................................			7
4	Set up, installation and reconditioning .........................................................			8
5	Operation		.........................................................................................................	9
	5.1	Layout ................................of the switches und buttons on the control console		9
	5.2	Commissioning...................................................................................................		9
	5.3	Description ....................................................and function of the components		10
		5.3.1 ..............................................................................................................	Translation table	10
		5.3.2 ....................................................................................................................	Patient chair	11
		5.3.3 .................................................................................................................	Phoropter arm	11
		5.3.4 .....................................................................Contact lens fitting table with trial lens tray		11
6	Care and maintenance ..................................................................................			12
	6.1	Care..................................................................................................................		12
	6.2	Maintenance.....................................................................................................		12
	6.3	Repairs .....................................................that can be carried out by the user		12
		6.3.1 ....................................................................Changing the bulb in the examination lamp		12
		6.3.2 ......................................................................................................................	Safety fuse	13
		6.3.3 ..............................................................................................................	Function defects	13
7	Warranty.........................................................................................................			14
8	Technical ...............................................................................................data			15
9	Other information..........................................................................................			22

Appendix: EC Declaration of conformity

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1 Introduction

bon E-20 SE

1 Introduction

Dear customer

Thank you for purchasing our refraction unit bon E-20 SE. Please read the operating instructions carefully before using the system. Keep these instruction manual safe for future use. Please observe the safety instructions.

If you have any further questions, please contact our customer helpline.

Meaning of the symbols in the operating instructions

Caution! Please observe safety instructions with this symbol to prevent personal danger or damage to property.

Important! Indicates particularly important information to maintain the function of the device/system or to extend its life.

Note! Indicates information for correct use so that errors may be avoided.

This publication may not be copied or transferred without prior agreement from bon Optic.

bon Optic reserves the right to make changes in the interest of technical development. These operating instructions are not subject to updating.

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2 Important information

bon E-20 SE

2 Important information

Manufacturer: bon Optic Vertriebsgesellschaft mbH · Stellmacherstr. 14 · D- 23556 Lübeck

2.1 Information about the device

Device description: bon E-20 SE

2.2 Intended purpose and classification

The bon E-20 SE refraction unit is used in conjunction with ophthalmological instruments such as slitlamps and opthalmometers. During use in an ophthalmic examination these devices are positioned in front of the patient.

According to the classification rules of the Medical Device Directive 93/42/EWG, the bon E-20 SE refraction unit is classified as a non invasive medical active product class 1.

2.3 Liability

The Refraction Unit is manufactured according to the recognized technical safety regulations and is tested to the strictest quality measures. The company bon Optic accepts responsibility for the safety, reliability and performance of the device only when:

Mounting, modification and commissioning are carried out by a person(s) authorised to do so by bon Optic.

The power supply to which the device is connected corresponds to the national legislation.

The device is only used in accordance with this instruction manual.

The user operates in accordance with the Medical Device Use Practice (MPBetreibV).

The manufacturer will not accept liability should the system be assembled, amended or commissioned by an unauthorised person, should it be improperly serviced, or should it be other than as described under 2.2 .

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2 Important information

bon E-20 SE

2.4 Scope of delivery

1 Piece Refraction Unit E-20 SE

(Your Refraction Unit may differ from that illustrated in 2.1 depending on the Configuration purchased.)

Fig. 2-1: bon E-20 SE with maximum parts and accessories

2 Pieces of Table connections for the table top devices (only supplied when a table is supplied).

1 Mains cable 1,5 m

1 Instruction manual

1 Set of fuses consisting of:

2 pieces	T 3,15 A	(for fuse F1, F4)
2 pieces	T 5,0 A	(for fuse F5, F6)
1 piece	T 4,0 A	(for fuse F2)
1 piece	T 6,3 A	(for fuse F3)

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3 Safety instructions

bon E-20 SE

3 Safety instructions

Please adhere to the legal guidelines for accident preventions and take note of the following safety instructions.

Set up and Installation:

The Refraction Unit must not be installed or used in damp rooms.

Please ensure the refraction unit is mounted on a level and stable surface.

The power must correlate to that shown on the Type label.

The maximum carrying capacity of the translation table (6) is 40 kg, 25 kg maximum can be placed in position 1 of the translation table.

To Operate:

Do not expose the system to any temperature extremes. The recommended usage temperature lies between + 10° and + 40° C.

Avoid dripping water and water spray.

The maximum carrying capacity of the patient chair (5) is 170 kg. This must not be exceeded.

When the translation table (6) and the contact lens fitting table (7) are swung into position. There is a scissor movement. This presents a risk of trapping!

The elevation column of the patient chair is not designed for continuous use. After continuous use for 60 seconds a cooling off period of 9 minutes must be adhered to.

Please note that neither the translation table (6) nor the contact lens fitting (7) should be allowed to hit the patient` legs.

Do not exert any unnecessary pressure on the contact lens table (e.g. Leaning with the hand).

Ensure that the phoropter arm (2) does not hit the patient (e.g. as the chair moves upwards).

Longer use of the examination lamp (3) can lead to a heating of the lamp housing. There is a danger of burning.

Other:

Do not pull the cable when removing the plug from the socket.

Position the cable so that there is no risk of walking on it or falling over it. Any other risk of damage to the cable must be avoided (e.g. sharp edges or strong heat).

The plug must be removed from the socket before carrying out repairs, maintenance or commissioning.

Fig. 3-1: Refraction Unit bon E-20 SE

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