What is the role of a Notified Body in the EU for testing products? Are testing labs and Notified Bodies the same entity?
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Where can manufacturers and importers have their FFP2 respirators certified? And what can distributors do to check the quality of FFP2 mask shipments?
How do you know whether the certificates provided by your trading partner are sufficient to sell face masks and other PPE in the EU?
Which testing labs can test medical protective equipment according to legal requirements?
What requirements must respirator masks and mouth/nose guards meet in order to be approved for sale in the EU?
