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EU approval for medical devices




  My company is developing a medical imaging product based on the 
  TP760. We are, of necessity, concerned about regulatory agency
  approval of all the stuff we sell in various markets around the world.

  Our problem is the CE mark approval that is stamped on the Thinkpad
  case. We can not tell what level of approval this represents, and don't
  know who to get in touch with within IBM to find out.

  Does anyone on this list know who we could talk to at IBM concerning
  European certifications?

  Thanks in advance.

       Don
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