For Europe:
The equipment described in this manual is in accordance with the requirements of the Medical
Device Directive 93/42/EEC.
Zilverstraat 1, 2718 RP
EC
REP
Zoetermeer, The Netherlands
TOSHIBA MEDICAL SYSTEMS EUROPE B.V.
Unauthorized modification of the product or configuration invalidates the CE Marking.
For other countries, please contact your local distributor.
LEGAL MANUFACTURER
1385, SHIMOISHIGAMI, OTAWARA-SHI, TOCHIGI-KEN 324-8550, JAPAN
No. 2B771-004EN*M
A-2
E