Fluke Biomedical 2MF Index User Manual

Page 4

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Return Procedure

All items being returned (including all warranty-claim shipments) must be sent freight-prepaid to our factory location. When you return
an instrument to Fluke Biomedical, we recommend using United Parcel Service, Federal Express, or Air Parcel Post. We also
recommend that you insure your shipment for its actual replacement cost. Fluke Biomedical will not be responsible for lost shipments
or instruments that are received in damaged condition due to improper packaging or handling.

Use the original carton and packaging material for shipment. If they are not available, we recommend the following guide for
repackaging:

ƒ

Use a double-walled carton of sufficient strength for the weight being shipped.

ƒ

Use heavy paper or cardboard to protect all instrument surfaces. Use nonabrasive material around all projecting parts.

ƒ

Use at least four inches of tightly packed, industry-approved, shock-absorbent material around the instrument.


Returns for partial refund/credit:

Every product returned for refund/credit must be accompanied by a Return Material Authorization (RMA) number, obtained from our
Order Entry Group at 1-800- 850-4608 or 1-440-248-9300.

Repair and calibration:

To find the nearest service center, goto

www.flukebiomedical.com/service

, or


In the U.S.A.:
Cleveland Calibration Lab
Tel:

1-800-850-4606

Email:

[email protected]


Everett Calibration Lab
Tel:

1-888-993-5853

Email:

[email protected]


In Europe, Middle East, and Africa:
Eindhoven Calibration Lab
Tel:

+31-402-675300

Email:

[email protected]


In Asia:
Everett Calibration Lab
Tel:

+425-446-6945

Email:

[email protected]

Certification

This instrument was thoroughly tested and inspected. It was found to meet Fluke Biomedical’s manufacturing specifications when it
was shipped from the factory. Calibration measurements are traceable to the National Institute of Standards and Technology (NIST).
Devices for which there are no NIST calibration standards are measured against in-house performance standards using accepted test
procedures.

WARNING

Unauthorized user modifications or application beyond the published specifications may result in electrical shock hazards or
improper operation. Fluke Biomedical will not be responsible for any injuries sustained due to unauthorized equipment
modifications.

Restrictions and Liabilities

Information in this document is subject to change and does not represent a commitment by Fluke Biomedical. Changes made
to the information in this document will be incorporated in new editions of the publication. No responsibility is assumed by
Fluke Biomedical for the use or reliability of software or equipment that is not supplied by Fluke Biomedical, or by its
affiliated dealers.

Manufacturing Location

The Index 2MF Pulse Oximeter Analyzer is manufactured in Everett, Washington by Fluke Biomedical, 6920 Seaway Blvd.,
Everett, WA, U.S.A.

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