Ivy Biomedical Systems 3000 Series Manuale utente

P/N 2811-00-20

User Responsibility

This product will perform in conformity with the description thereof contained in this Operation Manual and

accompanying labels and/or inserts, when assembled, operated, maintained and repaired in accordance with the

instructions provided. This product must be checked periodically. A defective Product should not be used. Parts that

are broken, missing, plainly worn, distorted or contaminated should be replaced immediately. Should such repair or

replacement become necessary, IVY Biomedical Systems, Inc. recommends that a telephone call or written request

for service advice be made to IVY Biomedical Systems, Inc. Service Department. This product or any of its parts

should not be repaired other than in accordance with instructions provided by IVY Biomedical Systems, Inc. trained

personnel. The product must not be altered without the prior written approval of IVY Biomedical Systems, Inc.

Quality Assurance Department. The user of this Product shall have the sole responsibility for any malfunction,

which results from improper use, faulty maintenance, improper repair, damage or alteration by anyone other than

IVY Biomedical Systems, Inc.

CAUTION: US Federal law restricts this device to sale by or on the order of a licensed medical practitioner.

Ivy Biomedical Systems, Inc. has declared that this product conforms with the Eurpean Council Directive

93/42/EEC Medical Device Directive when its used in accordance with the instructions provided in the Operation

and Maintenace Manual.

Ivy Biomedical Systems, Inc.

11 Business Park Drive

Branford, Connecticut 06405. USA

(203) 481-4183 y(800) 247-4614 yFAX (203) 481-8734

www.ivybiomedical.com e-mail:[email protected]

SM3000series

22Sep2005

2811-00-20 Rev.00

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Table of Contents

WARRANTY...................................................................................................................................................... iii

INTRODUCTION................................................................................................................................................1

SAFETY................................................................................................................................................................2

Electrical................................................................................................................................................................2

Explosion...............................................................................................................................................................2

Patient Connections..............................................................................................................................................3

MRI........................................................................................................................................................................3

Pacemakers ...........................................................................................................................................................3

Electrosurgery Protection....................................................................................................................................3

Defibrillation Protection......................................................................................................................................3

EMC.......................................................................................................................................................................3

Electromagnetic Compatibility IEC 60601-1-2:2001 ..............................................................................3

Description of Warning Labels ...........................................................................................................................8

MONITOR DESCRIPTION ...............................................................................................................................9

Classification.........................................................................................................................................................9

Control and Indicators.......................................................................................................................................10

Basic Keys..............................................................................................................................................10

Programmable Keys ...............................................................................................................................11

Menu Structures .....................................................................................................................................11

Display ...................................................................................................................................................15

Alarm Messages .....................................................................................................................................16

Rear Panel ..............................................................................................................................................16

Fuse Ratings ...........................................................................................................................................17

TESTING AND TROUBLESHOOTING.........................................................................................................18

MAINTENANCE AND CLEANING ...............................................................................................................23

Monitor................................................................................................................................................................23

Patient Cables.....................................................................................................................................................23

Preventive Maintenance.....................................................................................................................................23

ACCESSORIES..................................................................................................................................................24

ECG .....................................................................................................................................................................24

Disposal................................................................................................................................................................24

SPECIFICATIONS............................................................................................................................................25

BOARD LAYOUTS AND SCHEMATICS.......................................................................................................A

ASSEMBLIES DRAWINGS AND SPARE PART LISTS ..............................................................................B

Model 3000 Series Service Addendum i

Table of Contents

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ii Model 3000 Series Service Addendum

WARRANTY

All products manufactured by Ivy Biomedical Systems, Inc. under normal use, are warranted to be free from defects

in material and workmanship and to operate within published specifications, for a period of one year from date of

original shipment.

All accessories such as patient cables and lead wires, supplied by Ivy Biomedical Systems, Inc. under normal use,

are warranted to be free from defects in material and workmanship and to operate within published specifications,

for a period of 90 days from date of original shipment.

If an examination by Ivy Biomedical Systems, Inc. discloses such product(s) or component part(s) to have been

defective, then Ivy’s obligation is limited at Ivy’s option, to repair or replacement.

When a product or products need to be returned to the manufacturer for repair or examination, contact customer

service personnel at Ivy Biomedical Systems, to obtain a Return Material Authorization number (RMA #) and the

correct packing instructions:

Customer Service

Telephone: (203) 481-4183 or (800) 247-4614.

Fax: (203) 481-8734.

E-mail: [email protected]

All products being returned for warranty repair shall be shipped prepaid to:

Ivy Biomedical Systems, Inc.

11 Business Park Drive.

Branford, CT. 06405. USA.

Ivy will prepay the shipment of the repaired or replacement product to customer at Ivy’s expense.

Model 3000 Series Service Addendum iii

WARRANTY

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iv Model 3000 Series Service Addendum

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