1. PREFACE
Do not attempt to use this equipment without thoroughly reading and under-
standing these instructions.
1.1
Manufacturer
Manufacturer: Room 6319, Building 1, No.27, Yongwang Road, Daxing
Bioengineering and Medicine Industry Base Zhongguancun Science Park Daxing District
102629 Beijing PEOPLE'S REPUBLIC OF CHINA
Product Name
Device Type
1.2
Manufacturer's Responsibility
M&B (Beijing M&B Electronic Instruments, Co., Ltd) is responsible for the safety, reliability, and per-
formance of the AED7000 Semiautomatic External Defibrillator, only if the following conditions are
met:
Assembly operations, extensions, readjustments, modifications, or repairs are carried out by persons
authorized by M&B.
The AED7000 Semiautomatic External Defibrillator equipment is used in accordance with the
instructions for use.
1.3
User's Responsibility
The AED7000 Automated External Defibrillator is intended for use by personnel who are authorized
by a physician/medical director, and who have had training in the use of an AED.
The user should be completely knowledgeable of the information contained in the AED7000 Se-
miautomatic External Defibrillator Users Manual. As with all other electronic patient care monitor,
good clinical judgment should be used when operating the AED7000 Semiautomatic External
Defibrillator. To ensure patient safety and proper operation, use only manufacturer authorized parts
and accessories.
User must save all shipping containers and packaging materials. When shipping the AED7000 and
accessories for calibration, service, or upgrades, the original shipping containers and packaging ma-
terials must be used.
1.4
Contact and Technical Support
Please contact M&B if you have any questions regarding this notice
Telephone: +86 10 6125 3747
Fax: +86 10 6125 3794
Internet: www.mbelec.com
E-mail: service@mbelec.com
6 6
Automatic External Defibrillator
AED7000