Annex 1A and 1B of the Second Draft of the Proposal for a Directive on Waste
from Electrical and Electronic Equipment specifies categories and examples of
equipment that is covered by the Directive.
In the section for Medical Equipment Systems it specifies "Laboratory equipment
for in-vitro diagnostics", yet does not just specify Laboratory Equipment.
Why are they so specific to spell out "in-vitro diagnostics"? Does this imply
that they are not concerned about general laboratory equipment? Does anyone
know their intent?
All responses are appreciated.
regards
Joe Martin
P.E. Biosystems
[email protected]
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