Ec Declaration of Conformity: Product Model Standard Configuration Including: Classification (MDD, Annex Ix) : Iib

EC Declaration of Conformity
Product Portable patient Monitor

Model M9
Standard Configuration Including:
M9: ECG, SPO2, NIBP, IBP, TEMP, EtCO2, CO
Classification (MDD, Annex IX): IIb
We herewith declare that the above mentioned products meet the provisions of the following
EC Council Directives and Standards. All supporting documentation is retained under the
premises of the manufacturer and the notified body.
We have verified the mutual compatibility of the devices in accordance with the
manufacturers' instructions and have carried out their operations in accordance with these
instructions; and
We have packaged the system pack and supplied relevant information to users incorporating
relevant instructions from the manufacturers; and The whole activity is subjected to
appropriate methods of internal control and inspection.
Directives
General Applicable Directives:
Medical Device Directive: COUNCIL DIRECTIVE 93/42/EEC of June 14, 1993 concerning
medical devices (MDD 93/42/EEC).
Standards:
Harmonized Standards (published in the Official Journal of the European Communities)
applicable to this product are: EN ISO 9001, EN 46001, EN 1441, EN 980, IEC 878, EN
30993, EN 540, EN 60601-1, EN 60601-1-2, EN 60601-1-4, EN 475, EN 61157, ISO 1000,
EN 1041.
Notified Body:
TÜV Product Service GmbH, TÜV SÜddeutschland•TÜV Nord Groups Ridlerstrasse 65, D-
80339 Munich, Germany.
M9 Portable Patient Monitor I

This item is compliant with Medical Device Directive 93/42/EEC of June 14, 1993, a directive
of the European Economic Community.
Copyright
Version: VA2.1
Issued date: 2003/12/12
Statement
Edan owns all rights to this unpublished work and intends to maintain this work as
confidential. Edan may also seek to maintain this work as an unpublished copyright. This
publication is to be used solely for the purposes of reference, operation, maintenance, or
repair of equipment. No part of this can be disseminated for other purposes.
In the event of inadvertent or deliberate publication, Edan intends to enforce its rights to this
work under copyright laws as a published work. Those having access to this work may not
copy, use, or disclose the information in this work unless expressly authorized by Edan to do
so.
All information contained in this publication is believed to be correct. Edan shall not be liable
for errors contained herein nor for incidental or consequential damages in connection with the
furnishing, performance, or use of this material. This publication may refer to information and
protected by copyrights or patents and does not convey any license under the patent rights of
Edan, nor the rights of others. Edan does not assume any liability arising out of any
infringements of patents or other rights of third parties.
Content of this manual is subject to changes without prior notice.
Responsibility on the manufacturer party
Edan is responsible for safety, reliability and performance of this equipment only in the
M9 Portable Patient Monitor II

condition that:
 all installation, expansion, change, modification and repair of this equipment are conducted
by qualified personnel; and,
 applied electrical appliance is in compliance with relevant National Standards; and,
 the monitor is operated under strict observance of this manual.
 NOTE 
This equipment is not intended for family usage.
Warning
This monitor is not a device for treatment purpose.
It is important for the hospital or organization that employs this equipment to carry out a
reasonable maintenance schedule. Neglect of this may result in machine breakdown or injury
of human health.
Upon request, Edan may provide, with compensation, necessary circuit diagrams, calibration
illustration list and other information to help qualified technician to maintain and repair some
parts, which Edan may define as user serviceable.
M9 Portable Patient Monitor III

Warranty
Workmanship & Materials
Edan guarantees new equipment other than accessories to be free from defects in
workmanship and materials for a period of one year (six months for multi-site probes and
SpO2 sensor) from date of shipment under normal use and service. Edan's obligation under
this warranty is limited to repairing, at Edan’s option, any part which upon Edan's examination
proves defective.
THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ALL OTHER WARRANTIES,

EXPRESSED OR IMPLIED, INCLUDING WARRANTIES OF MERCHANT ABILITY OR
FITNESS FOR ANY PARTICULAR PURPOSE.
Exemptions
Edan's obligation or liability under this warranty does not include any transportation or other
charges or liability for direct, indirect or consequential damages or delay resulting from the
improper use or application of the product or the substitution upon it of parts or accessories
not approved by Edan or repaired by anyone other than a Edan authorized representative.
This warranty shall not extend to any instrument which has been subjected to misuse,
negligence or accident; any instrument from which Edan's original serial number tag or
product identification markings have been altered or removed, or any product of any other
manufacturer.
Safety, Reliability and Performance
Edan is not responsible for the effects on safety, reliability and performance of M9 Portable
Patient Monitor if:
■ assembly operations, extensions, re-adjusts, modifications or repairs are carried out by
persons other than those authorized by Edan.
■ M9 Portable Patient Monitor is not used in accordance with the instructions for use, or
the electrical installation of the relevant room does not comply with NFPA 70: National
Electric Code or NFPA 99: Standard for Health Care Facilities (Outside the United States,
the relevant room must comply with all electrical installation regulations mandated by the
M9 Portable Patient Monitor IV

local and regional bodies of government).
Return Policy
Return Procedure
In the event that it becomes necessary to return a unit to Edan, the following procedure
should be followed:
1. Obtain return authorization. Contact Edan Service Department and obtain a Customer
Service Authorization number. The number must appear on the outside of the shipping
container. Return shipments will not be accepted if the number is not clearly visible.
Please provide the model number, serial number, and a brief description of the reason for
return.
2. Freight policy. The customer is responsible for freight charges when equipment is
shipped to Edan for service (this includes customs charges).
Contact
Edan Instruments, Inc.

4/F New Energy Building, 2009# Nanyou Road,
Shenzhen, P.R.China
518054
Tel: 86-755-26062220
Fax: 86-755-26062022
E-mail: info@edan.com.cn
M9 Portable Patient Monitor V

Preface
This manual gives detailed description to M9 Portable Patient Monitor concerning its
performance, operation, and other safety information. Reading through this manual is the first
step for the user to get familiar with the equipment and make the best out of it.
Following symbols indicates some important facts that you have to pay special attention to:
Warning Points to be noted to avoid injury to the patient and the operator.
Caution Points to be noted to avoid damage to the equipment.
 NOTE  Points to be noted.

This manual is intended for persons who are trained in the use of this field and have adequate
experience in operation of monitoring equipment.
M9 Portable Patient Monitor VI

Ec Declaration of Conformity: Product Model Standard Configuration Including: Classification (MDD, Annex Ix) : Iib

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EC Declaration of Conformity

Product Portable patient Monitor

M9 Portable Patient Monitor I

Content of this manual is subject to changes without prior notice.

Responsibility on the manufacturer party

M9 Portable Patient Monitor II

M9 Portable Patient Monitor III

Workmanship & Materials

THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ALL OTHER WARRANTIES,

Safety, Reliability and Performance

M9 Portable Patient Monitor IV

Edan Instruments, Inc.

M9 Portable Patient Monitor V

Caution Points to be noted to avoid damage to the equipment.

 NOTE  Points to be noted.

M9 Portable Patient Monitor VI

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