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Fluke Biomedical DPM1B User Manual

Page 4

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Use the original carton and packaging material for shipment. If they are not available,

we recommend the following guide for repackaging:

Use a double–walled carton of sufficient strength for the weight being

shipped.

Use heavy paper or cardboard to protect all instrument surfaces. Use

nonabrasive material around all projecting parts.

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

1-440-498-2560.

Repair and calibration:

To find the nearest service center, go to

www.flukebiomedical.com/service

or

In the U.S.A.:

Cleveland Calibration Lab

Tel: 1-800-850-4608 x2564

Email:

[email protected]

Everett Calibration Lab

Tel: 1-888-99 FLUKE

(1-888-993-5853)

Email:

[email protected]

In Europe, Middle East, and Africa:

Eindhoven Calibration Lab

Tel: +31-40-2675300

Email:

[email protected]

In Asia:

Everett Calibration Lab

Tel: +425-446-6945

Email:

[email protected]

To ensure the accuracy of the Product is maintained at a high level,

Fluke Biomedical recommends the product be calibrated at least once every

12 months. Calibration must be done by qualified personnel. Contact your local

Fluke Biomedical representative for calibration.

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 DPM1B Pneumatic Transducer Tester is manufactured at Fluke Biomedical,

6920 Seaway Blvd., Everett, WA, U.S.A.