Under current regulations, specimen collection cards, including neonatal screening cards, which are to be used for human diagnostic tests, are classified as "other" IVD devices under the European IVD Directive and require the CE mark if sold within the European Union
All 903 specimen collection devices manufactured and printed by Whatman for neonatal testing in the EU undergo post-printing quality control and carry the CE mark
Whatman will assume no responsibility for the quality or performance of 903 collection devices converted, printed, or packaged by third party suppliers
Disclaimer : No part of this site constitute medical advice or nor it replaces any advice provided by healthcare adviser. We urge buyer to take advice from the designated healthcare adviser about usage of any product here or if it is suitable for the buyer. This site takes no responsibility of the consequences arising out of the usage of any product from this site. By buying products from this site, buyer agree that buyer has the knowledge of the usage of the product. All warranties implied or explicitly mentioned here are responsibility of the manufacturer of the product. We are not able to accept any insurance or Medicaid or Medical for any purchase. Our apologies for that inconvenience.
WARNING: There are products on this website which can expose you to chemicals known to the State of California to cause cancer and birth defects or other reproductive harm. For more information go to www.p65warnings.ca.gov.