Gima 32569 Handleiding

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M32506-M-Rev.5-02.21

PROFESSIONAL MEDICAL PRODUCTS

STETOSCOPI GIMA - GIMA STETHOSCOPES

STÉTHOSCOPES BIAURICULAIRES GIMA

ESTETOSCOPIOS GIMA - ESTETOSCÓPIO GIMA

GIMA STETHOSKOPE - GIMA SZTETOSZKÓP

STETOSKOPY GIMA - GIMA STETOSKOP

ΣΤΗΘΟΣΚΟΠΙΑ GIMA - GIMA

È necessario segnalare qualsiasi incidente grave vericatosi in relazione al dispositivo

medico da noi fornito al fabbricante e all’autorità competente dello Stato membro in cui

si p1-ha sede.

All serious accidents concerning the medical device supplied by us must be reported to

the manufacturer and competent authority of the member state where your registered of-

ce is located.

Il est nécessaire de signaler tout accident grave survenu et lié au dispositif médical que

nous avons livré au fabricant et à l’autorité compétente de l’état membre où on a le siège

social.

Es necesario informar al fabricante y a la autoridad competente del Estado miembro en el

que se encuentra la sede sobre cualquier incidente grave que haya ocurrido en relación

con el producto sanitario que le hemos suministrado.

É necessário noticar ao fabricante e às autoridades competentes do Estado-membro

onde -ele está sediado qualquer acidente grave vericado em relação ao dispositivo méd

ico fornecido por nós.

Jeder schwere Unfall im Zusammenhang mit dem von uns gelieferten medizinischen Gerät

muss unbedingt dem Hersteller und der zuständigen Behörde des Mitgliedsstaats, in dem

das Gerät verwendet wird, gemeldet werden.

A gyártónak, illetve a székhely szerinti tagállam illetékes hatóságának jelezni kell bármilyen

olyan súlyos balesetet, amely az általunk szállított orvostechnikai eszközzel kapcsolatban

történt.

Należy poinformować producenta i kompetentne władze danego Kraju członkowskiego o

każdym poważnym wypadku związanym z wyrobem medycznym naszej produkcji.

Det är nödvändigt att meddela tillverkaren och de behöriga myndigheterna i den berörda

medlemsstaten, om alla allvarliga olyckor som inträffat i samband med den medicintekni-

ska utrustning som levererats av oss.

Σε περίπτωση που διαπιστώσετε οποιοδήποτε σοβαρό περιστατικό σε σχέση με την ιατρική

συσκευή που σας παρέχουμε θα πρέπει να το αναφέρετε στον κατασκευαστή και στην

αρμόδια αρχή του κράτους μέλους στο οποίο βρίσκεστε.





32506 - 32508 - 32509 - 32511 - 32513 - 32515 - 32526

32527 - 32528 - 32542 - 32569 - 32570 - 32571 - 32572

32574 - 32575 - 32576 - 32577 - 49500 - 49501 - 49502

49503 - 49510 - 49511 - 49512 - 49513

Gima S.p.A.

Via Marconi, 1 - 20060 Gessate (MI) Italy

gima@gimaitaly.com - export@gimaitaly.com

www.gimaitaly.com

Made in Taiwan

4ENGLISH

These medical devices are intended for auscultation.

Bow adjustment

Position the eartubes so that

they are inclined at about 15°

and the eartips are in line with

the nose bridge, facing forward

with respect to you (see illus-

tration).

In this way the eartubes will be

aligned with the ear canal and

you will obtain a clear, sharp

sound.

Holding the eartubes in front

of you with one tube in each

hand, open them, separating

the tubes and inserting the

eartips in your ears.

Adjustment of the bow tension

If you feel uncomfortable or performance is poor, adjust the ten-

sion of the eartubes. Press the binaural eartubes against each

other gently to increase the tension, separate them to reduce it.

• Attention: an excessive tension could weaken the

bow.

• For best performance, it is important to use eartips

of a suitable size for your ears. This is particularly

important if you’re using soft conformable eartips.

Replacement of the diaphragm

Although the diaphragm is solid and planned to last long, it

could be necessary to replace it.

In this case proceed as follows:

• Remove the backing ring, paying attention not to damage it

(for screw models, counter clockwise rotate the ring), then pull

the diaphragm out.

• Fit the new diaphragm and reposition the backing ring making

sure that it is well xed (for screw models clockwise rotate the

ring).

5ENGLISH

Selection of frequency / cushion

for double-head models only

Rotating the chestpiece by 180°, it is possible to change the lis-

tening mode by opening (or indexing) the side you wish to use,

either the diaphragm or open bell: select the diaphragm to listen

to high frequencies, or the open bell to listen to low frequencies.

“If the diaphragm is open, the bell will be closed, blocking the

sound coming from the bell and vice versa. To determine which

of the two sides is active, position the eartips in your ears and

exert slight pressure on the diaphragm or on the hole of the bell.

Cleaning and maintenance

Regular and periodic cleaning will ensure best performance

over time:

• Keep away from extreme heat and cold, solvents and

oils.

• Do not submerge the product in liquids and do not sub-

ject it to sterilisation processes.

• Disinfect the product after each use, using a 70% iso-

propyl alcohol solution.

• Avoid damage to the product caused by sharp objects.

• Regularly unscrew the eartips to keep them clean.

Clean the eartips (and various parts of the product, if

necessary) with alcohol or soapy water and dry them

completely before reassembling them. Make sure the

eartips have been securely retted to the ends of the

eartubes.

• Do not use the product disassembled (e.g. without eart-

ips) and/or in the event of visible damage

GIMA WARRANTY TERMS

The Gima 12-month standard B2B warranty applies.

Product specificaties

Merk:	Gima
Categorie:	Niet gecategoriseerd
Model:	32569
Kleur van het product:	Zwart
Soort:	Akoestische stethoscoop
Type verpakking:	Doos
Lengte:	630 mm
Membraan diameter:	45 mm
Niet-koelrand:	Ja
Membraandiameter:	30 mm