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1
CARRELLO TRIS
TRIS TROLLEY
CHARIOT TRIS
WAGEN TRIS
CARRO TRIS
CARRINHO TRIS
• È necessario segnalare qualsiasi incidente grave verificatosi in relazione al
dispositivo medico da noi fornito al fabbricante e all'autorità competente dello Stato
membro in cui si ha sede.
• A ll 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 office is located.
• I l 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.
• J eder 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.
• E s 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 notificar ao fabricante e às autoridades competentes do Estado-membro
onde ele está sediado qualquer acidente grave verificado em relação ao dispositivo
médico fornecido por nós.
27438
Gima S.p.A.
Via Marconi, 1 - 20060 Gessate (MI) Italy
gima@gimaitaly.com - export@gimaitaly.com
www.gimaitaly.com
Made in Italy
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Summary of Contents for Gima Tris
- Page 1 CARRELLO TRIS TRIS TROLLEY CHARIOT TRIS WAGEN TRIS CARRO TRIS CARRINHO TRIS • È necessario segnalare qualsiasi incidente grave verificatosi in relazione al dispositivo medico da noi fornito al fabbricante e all’autorità competente dello Stato membro in cui si ha sede. • A ll 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 office is located. • I l 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. • J eder 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. • E s 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 notificar ao fabricante e às autoridades competentes do Estado-membro onde ele está sediado qualquer acidente grave verificado em relação ao dispositivo...
- Page 2 You should carefully read this manual before using this medical device. DESCRIPTION The New Tris is a practical trolley with three shelves made painted sheet metal, equipped with 4 nylon castors and two lateral handles for easy moving, suitable to support and transport small electromedical instruments.
- Page 3 ENGLISH DETAIL A ➞ INNER EXTERNALLY Screw the shelf to the structure using the screws supplied with the 2 Allen key. Having fixed the three shelves on the same side, go to next side. 2. Once the shelves have been assembled, turn the trolley upside down by plcing the fi rst shlef and the black rubbers on the work surface and moving on to fi xing the wheels.
- Page 4 Keep away from sunlight Keep in a cool, dry place with Regulation (EU) 2017/745 Product code Consult instructions for use Manufacturer Caution: read instructions Lot number Medical Device (warnings) carefully GIMA WARRANTY TERMS The Gima 12-month standard B2B warranty applies.
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