RF Regulatory

RF Communications FACTS :

The source in a communications system must produce digital information only that will be transmitted by the transmitter. N The source in a communications system must produce digital information only that will be transmitted by the transmitter.

"This has been a whole new venture for me and your professional, collaborative and creative approach has made the design process much easier than I had ever anticipated."

""This has been a whole new venture for me and your professional, collaborative and creative approach has made the design process much easier than I had ever anticipated."

"This has been a whole new venture for me and your professional, collaborative and creative approach has made the design process much easier than I had ever anticipated."

PCS certified medical products have been universally accepted in the US and Canada. PCS tests and certifies to:

  • • UL60601-1
  • • AAMIES60601-1
  • • CSA C22.2 No.601.1
Most Common SAR Test Standards that are used::
  • • OET Bulletin 65, Edition 97-01 (August 1997)
  • • Supplement C, Edition 01-01 to OET Bulletin 65,Edition 97-01
  • • IEEE Standard 1528 (2003) including Amendment 1
  • • EN 62369-1:2009
  • • EN 50360 (2001) (August 1997)
  • • EN 62209-1 (2006)
  • • IEC 62209-1 (Feb 2005)
  • • IEC 62209-2 (2010)
  • • ANSI C95.1:2005 +A1:2010
  • • EN 50364 (2001)
  • • EN 50371 (2002)
For interfnational safety certification requirements, PCS tests and certifies to:
  • • EN 60601-1
  • • EN 60601-2-XX
  • • IEC 60601-1
  • • IEC 60601-2-XX
    The 60601 series of standards consists of 60601-1 and 60601-2-XX. The Part 1 applies to all medical products while the Part 2 address specific requirements fo a particular type of medical device. There are over 40 Part 2s. The -XX is a number from 1 to 40+, representing the applicable Part 2.
  • EMC
    Medical EMC testing perfromed by PCS is typically to EN/IEC 60601-1-2 for most devices. Additions and/or deviations to the requirements of 60601-1-2, as published in the appropriate EN/IEC 60601-2-XX for particular devices, may also be applicable.
  • • ANSI ISO 14708-3 - Implants for surgery - Acive implatable medical devices - Part 3: implantable nerostimulators