Hologic PCB01647 RFID interface board for Selenia Dimensions / 3Dimensions Product Line User Manual 3Dimensions System User Guide
Hologic Inc RFID interface board for Selenia Dimensions / 3Dimensions Product Line 3Dimensions System User Guide
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Contents
- 1. User manual_3 Dimensions RFID_Updates EN part 1
- 2. User manual_3 Dimensions RFID_Updates EN part 2
User manual_3 Dimensions RFID_Updates EN part 1
































![3Dimensions System User GuideChapter 2: General InformationPage 20 MAN-05085-002 Revision 002 DRAFT Preview Copy-Generated May 30, 20182.6.2 Compliance StatementsThe manufacturer states this device is made to meet the following requirements: Medical – Applied electromagnetic radiation equipment as to electrical shock, fire and mechanical hazards only in accordance with ANSI/AAMI ES60601-1 (2005) and CAN/CSA-C22.2 No. 60601-1 (2008) •CAN/CSA - ISO 13485-03 Medical Devices – Quality Management Systems – Requirements for Regulatory Purposes (Adopted ISO 13485:2003 second edition, 2003-07-15) •CAN/CSA C22.2 NO. 60601-1-08 Medical Electrical Equipment – Part 1: General Requirements for Basic Safety and Essential Performance (Adopted IEC 60601-1:2005, third edition, 2005-12), includes Corrigendum 1:2011 •EN 60601-1:2006 Medical Electrical Equipment. General Requirements for Basic Safety and Essential Performance •ETSI EN 300 330-1: V1.3.1, and ETSI EN 300 330-2: V1.5.1: 2006—Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Radio equipment in the frequency range 9 kHz to 25 MHz and inductive loop systems in the frequency range 9 kHz to 30 MHz •ETSI EN 301 489-1: V1.6.1, and ETSI EN 301 489-3: V1.8.1: 2008—Electromagnetic compatibility and Radio spectrum Matters (ERM); ElectroMagnetic Compatibility (EMC) standard for radio equipment and services •FCC, 47 CFR Part 15, Subpart C, Section 15.225: 2009 •FDA, 21 CFR [Parts 820, 900 and 1020] •IEC 60601-1 Ed. 3.0:2005 Medical Electrical Equipment – Part 1: General Requirements for Basic Safety and Essential Performance •IEC 60601-1-2 Ed. 3.0:2007 Medical Electrical Equipment – Part 1-2: General Requirements for Basic Safety and Essential Performance - Collateral Standard: Electromagnetic Compatibility – Requirements and Tests •IEC 60601-1-3 Ed. 2.0:2008 Medical Electrical Equipment – Part 1-3: General Requirements for Basic Safety and Essential Performance –Collateral Standard: Radiation Protection in Diagnostic X-Ray Equipment •IEC 60601-2-28 Ed. 2.0:2010 Medical Electrical Equipment - Part 2-28: Particular Requirements for the Basic Safety and Essential Performance of X-ray Tube Assemblies for Medical Devices •IEC 60601-2-45 Ed. 3.0:2011 Medical Electrical Equipment – Part 2-45: Particular Requirements for Basic Safety and Essential Performance of Mammographic X-Ray Equipment and Mammographic Stereotactic Devices •RSS-210: Issue 7, 2007 Radio Standards Specification Low-power License-exempt Radiocommunication Devices: Category I Equipment •ANSI/AAMI ES60601-1:2005 (IEC 60601-1:2005, MOD) Medical Electrical Equipment, Part 1: General Requirements for Basic Safety and Essential Performance, includes amendment (2010)](https://usermanual.wiki/Hologic/PCB01647.User-manual-3-Dimensions-RFID-Updates-EN-part-1/User-Guide-3872294-Page-36.png)






























































