(c)
the defective used EEE for professional use, such as medical devices or their parts, is sent to the producer or a third party acting on his behalf for root cause analysis under a valid contract, in cases where such an analysis can only be conducted by the producer or third parties acting on his behalf.
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Source: EUR-Lex (Cellar) · retrieved 2026-09-29 · Text as consolidated on 2024-04-08; changes after this date are not shown.