EPC500ST-INS-LAB-RevA21 4
INTRODUCTION — A WORD FROM GF HEALTH PRODUCTS, INC.
This manual contains important information on proper use and maintenance of the Hausted
EPC500ST Procedure Chair. All personnel involved in the use and maintenance of this equipment
must carefully review and comply with the warnings, cautions and instructions contained in this
manual. These instructions are important to protect the health and safety of personnel operating
the model EPC500ST Procedure Chair, and should be retained in a conveniently accessible area for
quick reference.
Complete instructions for uncrating and putting your new equipment in service, as well as
equipment drawings, have been furnished. If missing, contact GF Health Products, Inc. for
replacement copies, giving the serial number and model number of the unit.
GF Health Products, Inc. carries a complete line of accessories for use with these chairs; your
representative will gladly review these with you.
Indications for Use
The Hausted EPC500ST Procedure Chair is intended for use in patient treatment, transport or
recovery. It has a radiolucent back for X-ray imaging capabilities of 20" x 25
1
/
2
" (50.8 cm x 64.8 cm)
width x height with a range of 0° to 90°. The product has an expected service life of five years.
The chair’s back can be positioned from sitting to supine. Height positioning, as well as back,
seat, and leg section adjustment, is electric / battery powered and is activated with a pendant.
The motorized leg extension is controlled by a switch underneath the footrest end. Four
advanced-steer casters allow maximum mobility and maneuverability, with control through either
pendant or manual operation.
Service Information
A thorough preventive maintenance program is essential to safe and proper unit operation. This
manual contains maintenance schedules and procedures which should be followed for satisfactory
equipment performance.
We encourage you to contact GF Health Products, Inc. with maintenance concerns.
Advisory
A listing of the safety precautions to be observed when operating and servicing this equipment
can be found in Section 1 of this manual. Do not operate or service the equipment until you
have become familiar with this information. Any alteration of this equipment not authorized or
performed by GF Health Products, Inc., could affect its operation, will void the warranty, could
violate national, state, and local regulations, and could jeopardize your insurance coverage.
Info: Column 1 below applies only if product was purchased outside the U.S.
EC
REP
EC Authorized
Representative:
CEpartner4U BV
ESDOORNLAAN 13
3951DB MAARN
The Netherlands
+31(0)6 516 536 26
Manufactured by:
GF Health Products, Inc.
One Graham-Field Way
Atlanta GA 30340-3140
1.770.368.4700 Main
1.770.368.2386 Fax
www.grahamfield.com
www.Hausted.com
Info: The base language of this document is ENGLISH. Any translations must be made from
the base language document.
Class 1 Equipment
Type B Equipment
Equipment not suitable for use
in the presence of flammable
anesthetic mixture with air or
oxygen or nitrous oxide.
IPX5 (Water-resistant)
Not suitable for continuous
operation (Duty Cycle:
5% 1 Min in 19 Min on Battery;
10% 2 Min in 18 Min on Mains
Power)
