![Terumo BCT Trima Accel Скачать руководство пользователя страница 329](http://html1.mh-extra.com/html/terumo-bct/trima-accel/trima-accel_service-manual_1090436329.webp)
Symbols and Certification
Table 6-29: Symbols and Certification
Symbol
Definition
Note:
Some symbols appear on the Trima Accel machine label, some appear on Trima Accel disposable kit labels, and others
appear on both labels.
Device is manufactured in conformance with the European Council Directive 93/42/
EEC of June 14, 1993, concerning medical devices.
This mark with the Notified Body Number 0086 indicates the approval by the British
Standards Institute for these devices within the European Community.
Device is certified by CSA International in accordance with applicable U.S. and
Canadian standards for conformance with the requirements of CAN/CSA-C22.2 No.
601.1-M90, CAN/CSA-C22.2 No. 1010.2.20-94, and UL 60601-1, as well as the
applicable respective amendments to these standards.
This symbol indicates that the connection of the Applied Part, or the part of the
disposable that comes in physical contact with the donor in normal use, is
electrically isolated from other parts of the Medical Electrical Equipment. In such a
case when any unintended voltage originating from an external source is connected
to the donor (that is, applied between the donor connection and earth), this
isolation is sufficient to ensure that no current higher than the allowable donor
leakage current will flow.
Indicates the European Authorized Representative of the product when
accompanied by the name of the European Authorized Representative.
Indicates the manufacturer of the product when accompanied by the name of the
manufacturer.
Indicates the date of manufacture (or sterilization date, if the product is sterile)
when accompanied by a specific date.
Indicates the product catalog number when accompanied by a number.
Indicates the product serial number.
This symbol indicates that consultation of the accompanying documents prior to
equipment operation is critical to the safe operation of the device.
Indicates that the equipment is subject to directive 2002/96/EC concerning waste
electrical and electronic equipment (WEEE) and must be disposed of accordingly.
Specifications
6-26
Trima Accel
®
Automated Blood Collection System • Service Manual
Содержание Trima Accel
Страница 1: ...Trima Accel Automated Blood Collection System Service Manual...
Страница 2: ...Trima Accel Automated Blood Collection System Service Manual Part No 777095 548 2015 09...
Страница 10: ...1 Operational Description Trima Accel Automated Blood Collection System Service Manual 1 1...
Страница 62: ...2 System Description Trima Accel Automated Blood Collection System Service Manual 2 1...
Страница 100: ...Linear Actuator System Trima Accel Automated Blood Collection System Service Manual 2 39...
Страница 133: ...System Description 2 72 Trima Accel Automated Blood Collection System Service Manual...
Страница 134: ...3 Software Description Trima Accel Automated Blood Collection System Service Manual 3 1...
Страница 261: ...Software Description 3 128 Trima Accel Automated Blood Collection System Service Manual...
Страница 262: ...4 Troubleshooting Trima Accel Automated Blood Collection System Service Manual 4 1...
Страница 288: ...5 Maintenance and Calibration Trima Accel Automated Blood Collection System Service Manual 5 1...
Страница 303: ...Maintenance and Calibration 5 16 Trima Accel Automated Blood Collection System Service Manual...
Страница 304: ...6 Specifications Trima Accel Automated Blood Collection System Service Manual 6 1...
Страница 333: ...Specifications 6 30 Trima Accel Automated Blood Collection System Service Manual...
Страница 339: ...Index 6 Trima Accel Automated Blood Collection System Service Manual...