Visitor T30 C-DR
User's Manual
[File: 218899-01-01-B.docx]
Page 5/74
1
CREDITS
1.1
Compliance
This medical device is in compliance with the Medical Device Directive 93/42/EC
and its revised versions.
The medical device, hereafter called equipment, has been classified in class IIb
according to annex IX rule 10 of the directive mentioned above.
1.2
Manufacturer
The Manufacturer (according to MDD 93/42/EC and its revised versions) of the equipment is:
Villa Sistemi Medicali
Via delle Azalee, 3
20090 Buccinasco, MI (Italy)
Tel.: +39-02- 48.859.1
Fax: +39-02-48.81.844
e-mail: [email protected]
Information about the compliance can be required to the Manufacturer.
1.3
Distributor
The Distributor of the equipment is:
Villa Sistemi Medicali
Via delle Azalee, 3
20090 Buccinasco, MI (Italy)
Tel.: +39-02- 48.859.1
Fax: +39-02-48.81.844
e-mail: [email protected]
1.4
Publishing details
Published by the Manufacturer.
The Manufacturer reserves the right to modify this User's Manual and the equipment here described.
The equipment specifications are subject to variations without notice. Nothing written in this User's Manual
can be considered as an offer, warranty, promise or contractual condition, nor should it be so.
1.5
Copyright
Translations from the original instructions in Italian language.
No part of this User's Manual may be reproduced or transmitted in any form without permission in writing
from Manufacturer.
The software included in the equipment belongs to the Manufacturer. Upon receipt of the equipment, the user
acquires only the right to use the software.
This right is neither exclusive nor transferable.
It is also necessary to seek a written permission to the Manufacturer before making changes for the use of the
equipment for purposes other than those established.
