Richard Wolf
2320 Telescope Warmer Instruction Manual Index : 10-04-4.0
Instruction Manual
19 Pages
Preview
Page 1
Instruction Manual Telescope Warmer 2320
Your dealer
HA--E155 / Index: 10--04--4.0 / ÄM: KG 04--243
Important general instructions for use Ensure that this product is only used as intended and described in the instruction manual, by adequately trained and qualified personnel, and that maintenance and repair is only carried out by authorized specialized technicians. Operate this product only in the combinations and with the accessories and spare parts listed in the instruction manual. Use other combinations, accessories and wearing parts only if they are expressly intended for this use and if the performance and safety requirements are met. Reprocess the products before every application and before returning them for repair as required by the instruction manual in order to protect the patient, user or third parties. Subject to technical changes! Due to the further development of our products, illustrations and technical data may deviate slightly from the data in this manual.
CAUTION - USA only: Federal law restricts this unit to be used or sold, except under the supervision of a medical doctor.
GERMANY RICHARD WOLF GmbH D--75438 Knittlingen Pforzheimerstr. 32 Tel.: (..49)--(0)7043--35--0 Fax:(..49)--(0)7043--35300 MANUFACTURER
USA RICHARD WOLF Medical Instruments Corp. 353 Corporate Woods Parkway Vernon Hills, Illinois 60061 Tel.: 847--913 1113 Fax: 847--913 1488
UK RICHARD WOLF UK Ltd. Waterside Way Wimbledon SW 17 0HB Tel.: 020--8944 7447 Fax: 020--8944 1311
E--mail: [email protected] Internet: www.richard--wolf.com
E--mail: sales&[email protected] Internet: www.richardwolfusa.com
E--mail: [email protected] Internet: www.richardwolf.uk.com
BELGIUM N.V. Endoscopie RICHARD WOLF Belgium S.A. Industriezone Drongen Landegemstraat 6 B--9031 Gent --Drongen Tel.: +32 9.280.81.00 Fax: +32 9.282.92.16
FRANCE RICHARD WOLF France S.A.R.L. Rue Daniel Berger Z.A.C. La Neuvillette F--51100 Reims Tel.: +33 3.26.87.02.89 Fax: +33 3.26.87.60.33
AUSTRIA RICHARD WOLF Austria Ges.m.b.H. Wilhelminenstraße 93 a A--1160 Wien Tel.: +43 1-- 405 51 51 Fax: +43 1-- 405 51 51--45
E--mail: [email protected]
E--mail: [email protected]
E--mail: [email protected] Internet: www.richard--wolf.at
HA--E155
0
Symbol
Designation OFF (disconnection from power supply) ON (connection to power supply) Caution, observe ACCOMPANYING DOCUMENTS!
8033.90
Operate only with tube inserts
Fuse A Registered Trademark of ETL, a Recognized Testing Laboratory, listing compliance as Medical Electrical Equipment to standard UL 60601-1 and CAN/CSA C 22.2 No. 601.1 Identification in conformity with Medical Devices Directive 93/42/EEC only valid if the product and/or packaging is marked with this symbol. Products of category IIa and above, as well as sterile products or products with measuring function of category I, are additionally marked with the code number of the notified body (0124)
SAFETY INSTRUCTIONS: A second telescope warmer should be at hand if the device fails. The tube inserts are not delivered in sterile condition. Before every use the tube inserts must be reprocessed as described in chapter 5.
2.1.1 .
3a
Combinations IMPORTANT!
In addition to this instruction manual follow the manuals of the products used in combination with this product.
HA-E 155
2.1.2
General requirements on products/components of a combination The general requirements depend on whether the products/components are inside or outside the patient environment. Patient environment
R = 1.5 m h = 2.5 m Patient environment
Acc. to UL 60601--1: R = 1.83 m (6 feet) ; h = 2.29 m (71/2 feet)
Medically used room Inside the patient environment
MP
MP
µ
µ
MP
NMP
µ
µ
MP
NMP
µ
**
outside the patient environment
Non--medically used room
Requirements / measures Leakage currents to clause 19 IEC/EN 60601--1--1 *
--
--
--
--
--
a) additional protective earth connection (to be clarified with manufacturer), or
MP
b) with additional isolating transformer **
NMP
µ MP
NMP
µ
µ
--
--
MP
MP or NMP
µ
µ
additional isolating transformer according to IEC/ EN 60601--1--1 **
additional separating device according to IEC/ EN 60601--1--1
a) common protective earth connection, or b) additional protective earth connection (to be clarified with manufacturer), or c) additional separating device (to avoid earth/ground loops in the case of a potential difference) Functional connection
µ power supply grid
MP NMP
= medical electrical device according to IEC/ EN 60601-1, UL 60601-1, CSA C22.2 No. 601 = non-medical electrical device in accordance with the relevant product-specific IEC/ EN/ UL/ IEC standards
* If connected via a joint mains/power cord under normal conditions the earth leakage current of the system must not exceed 500 µA (300 µA for systems in acc.with UL 60601-1).
** e.g. Richard Wolf Video Trolley with ”isolating transformer”.
HA-E 155
3b
2.1.3 .
2.2
Specific requirements on the products/components of a combination IMPORTANT! Persons combining products to form a system are responsible for not impairing the system’s compliance with the performance and safety requirements, and that the technical data and the intended use are adequately fulfilled. Electromagnetic interference or other types of interference occurring between this product and other products can cause failures or malfunctions. When selecting the system components ensure that they meet the requirements for the medical environment they are used in, in particular IEC/ EN 60601-1-1. In case of doubt contact the manufacturer(s) of the system components. Do not touch connecting devices for electrical connections between the different components (such as signal input and output connections for video signals, data exchange, control circuits, etc.) and the patient at the same time.
Electromagnetic compatibility (EMC)
NOTE: The device or system in the following called product always relates to the Telescope Warmer 2320 Guidance and manufacturer’s declaration - electromagnetic emissions The product is intended for use in the environment specified below. The user should assure that the product is used in such an environment. Emissions measurement/test
Compliance
Electromagnetic environment -- Guidance
HF emissions to CICPR 11
Group 1
The product uses HF energy for its internal function. The HF emission level is extremely low and it is not likely to cause any interference in nearby electronic equipment.
HF emissions to CISPR 11
Class B
Harmonic emissions to IEC 61000--3--2
Class A
In conformity with IEC 61000--3--3 “Voltage fluctuations / flicker emissions”
The product is suitable for use in all establishments, including domestic establishments and those directly connected to the public low--voltage power supply network that supplies buildings used for domestic purposes.
Guidance and manufacturer’s declaration - electromagnetic immunity The product is intended for use in the environment specified below. The user should assure that the product is used in such an environment. Immunity tests
IEC 60601 test level
Compliance
Electromagnetic environment -- guidance
Electrostatic Discharge (ESD) to IEC 61000--4--2
± 6 KV contact ± 8 KV air
Yes
Floors should wood, concrete or ceramic tile. If the floors are covered with synthetic material, the releative humidity should be at least 30%.
Electrical fast transients, bursts to IEC 61000--4--4
± 2 KV for power supply lines ± 1 KV for input/output lines
Yes
Mains/line power quality should be that of a typical commercial or hospital environment.
Surge voltage (surges) to IEC 61000--4--5
± 1 KV differential mode ± 2 KV common mode
Yes
Mains/line power quality should be that of a typical commercial or hospital environment.
Voltage dips, short interruptions and voltage variations on power supply input lines to IEC 61000--4--11
Voltage dip for 0.5 cycle > 95% UT * Voltage dip for 5 cycles > 60% UT * Voltage dip for 25 cycles > 30% UT * Voltage dip for 5 sec > 95% UT *
Yes
Mains/line power quality should be that of a typical commercial or hospital environment. If the user of the product requires continued operation during power mains/line interruptions it is recommended that the product be powered from an uninterruptible power supply or battery.
Power frequency (50/60 Hz) magnetic field, to IEC 61000--4--8
3 A/m
Yes
Power frequency magnetic fields should be at levels characteristic of a typical location in a commercial or hospital environment.
* NOTE: UT is the line/mains voltage prior to application of the test level.
3c
HA-E 155
Guidance and manufacturer’s declaration - electromagnetic immunity for products that are not life-supporting The product is intended for use in the environment specified below. The user should assure that the product is used in such an environment. Immunity test
Compliance level
IEC 60601 test levels
Electromagnetic environment -- guidance
Portable and mobile RF communications equipment should be used no closer to any part of the product, including cables, than the recommended separation distance calculated from equation applicable to the frequency of the transmitter. Recommended separation distance:
d = 1.2 p P d = 1.2 p P for 80 MHz to 800 MHz d = 2.3 p P for 800 MHz to 2.5 GHz
Conducted HF interference to IEC 61000--4--6
3 Vrms 150kHz to 80 MHz
Radiated HF interference to IEC 61000--4--3
3 V/m 80 MHz to 2.5 GHz
Yes
REMARKS:
P = Nominal power output rating of the transmitter in watts (W) (according to the transmitter manufacturer)
d = recommended separation distance in meters (m) Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey1, should be less than the compliance level in each frequency range2. Interference may occur in the vicinity of devices with the following symbol:
At 80 MHz and 800 MHz the higher frequency range applies. These guidelines may no apply in all situations, as the propagation of electromagnetic waves is affected by absorption and reflexion from buildings, objects and people.
1 = The field strength of fixed transmitters (e.g. base stations for radio telephones, land mobile radios, amateur radio, radio broadcast and TV broadcast, ...), cannot be predicted theoretically with accuracy. To assess the EMC environment due to fixed transmitters an electromagnetic site survey should be conducted. If the measured field strength in the location in which the product is used exceeds the applicable compliance level above, the product should be observed to verify normal operation. If abnormal performance is observed, additional measures may be required, such as reorienting or relocating the product. 2 = Over the frequency range between 150 kHz and 80 MHz the field strength should be below 3 V/m.
The recommended separation distances between portable and mobile HF telecommunication devices and devices which are not life-supporting The product is intended for use in an electromagnetic environment with HF disturbances are controlled. The user can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile HF telecommunications equipment and the product. Separation distance as a function of transmitter frequency (m)
Rated nominal output power of the transmitter (Watts)
150 kHz to 80 MHz
80 MHz to 800 MHz
800 MHz to 2.5 GHz
0.01
0.12
0.12
0.23
0.1
0.38
0.38
0.73
1
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
d = 1.2 p P
d = 1.2 p P
d = 2.3 p P
For transmitters rated at a nominal output power not listed in the table above, the recommended separation distance (d) in meters (m) can be determined using the applicable equation (observe frequency). P = nominal power of the transmitter in Watts (W). REMARKS: At 80 MHz and 800 MHz the higher frequency range applies. These guidelines may no apply in all situations. Electromagnetic propagation is affected by absorption and reflexion from buildings, objects and people.
HA-E155
3d
CAUTION! Danger of faults and malfunctions. To guarantee the safety of the user, the patient and others use only accessories and spare parts specified by the manufacturer of this product. Other accessories or spare parts can cause the emission of increased electromagnetic radiation or reduced immunity against interference.
. IMPORTANT!
Medical devices are subject to special precautions with regard to electromagnetic compatibility (EMC). Make sure you observe the notes on EMC for installation and operation. Medical electrical devices can be influenced by mobile HF communication devices. If it is necessary to stack the devices or place them next to each other and HF interference is observed, make sure you observe the intended use of the devices.
3e
HA-E 155
7
Technical data
7.1
Technical data of device Voltage
Frequency
Current rating A
Fuse
Hz
Power consumption VA
V µ
2320.001
220 - 240
50/60
240
1.0
T 1.25 H
2320.002
100 - 127
50/60
165
1.3
T 1.6 H
Model/type
Electromagnetic compatibility (EMC) to
IEC / EN 60601-1-2
Medical Devices Directive 93/42/EC
Category I
Group in acc. with MedGV
3
Safety class in acc. with EN/IEC 60601-1; (UL 60601-1 / CSA C22.2 No.601.1 - for USA)
I
Degree of protection against the ingression of liquids
IP 20 (not protected)
Duty type
Continuous operation This device is not protected against explosions (Do not operate this device in flammable environments)
Degree of protection if used in the presence of flammable gasses Weight
3.7 kg (8.2 lbs)
Dimensions WxHxD
7.2
A
205 mm x 124 mm x 314 mm
Operating, storage, transport and shipping conditions
Operating conditions
+ 10°C to + 40°C , 30% to 75% rel. humidity atmospheric pressure 700 hPa to 1060 hPa
Storage, transport and shipping conditions
- 20°C to + 60°C , 10% to 90% rel. humidity, atmospheric pressure 700 hPa to 1060 hPa
.
7.3
To protect the products from damage during transport and shipment we recommend using the original packaging material.
Spare parts and accessories Items
Model/type
Designation Spare parts
1
64068.004
Fuse T 1.6 H (pack of 10St.)
1
64068.003
Fuse T 1.25 H (pack of 10)
1
2440.03
Power cord (Europe), 3.0 m
1
8033.90
Tube insert
1
15135.036
Screw cap Accessories
1
6.08
Cleaning brush ' further accessories on request
HA-E 155
8
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