User's Instructions

10-7
WEEE (The Waste Electrical and Electronic Equipment Directive
This symbol on the product(s) and / or accompanying documents means that used electrical and
electronic products should not be mixed with general household waste. For proper treatment,
recovery and recycling, please take this product(s) to designated collection points where it will
be accepted free of charge.
Alternatively, in some countries you may be able to return your products to your local retailer
upon purchase of an equivalent new product.
Disposing of this product correctly will help save valuable resources and prevent any potential
negative effects on human health and the environment, which could otherwise arise from inappropriate waste
handling.
Please contact your local authority for further details of your nearest designated collection point.
Penalties may be applicable for incorrect disposal of this waste, in accordance with your national legislation.
For business users in the European Union:
If you wish to discard electrical and electronic equipment, please contact your dealer or supplier for
further information.
Information on Disposal in other Countries outside the European Union:
This symbol is only valid in the European Union. If you wish to discard this product please contact your
local authorities or dealer and ask for the correct method of disposal.
All Other Symbol and Labeling Information
For questions or additional information about symbols that appear in this document or on packaging labels,
please see www.mammotome.com.
How Supplied
The Mammotome revolve Probes, Specimen Management Systems, Vacuum Tubing Sets, Probe Guides, and
Vacuum Canisters are for single-patient use. Discard into an appropriate container after use. All other system
components are supplied non-sterile and should be disposed of in accordance with applicable local regulations.
For information on material content, contact Devicor Medical Products, Inc.
Responsibility of the Manufacturer
Devicor Medical Products, Inc. is responsible for the safety, reliability, and performance of this equipment
only if:
• The person installing the device ensures that the installation, inspection, and any required testing are
performed in accordance with the instructions in this manual.
• Persons authorized by Devicor Medical Products, Inc. carry out any and all service, repair, and upgrade
operations.
• The equipment is used in accordance with the Mammotome revolve Dual Vacuum-Assisted Biopsy
System Operator’s Manual.