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Seitens der Europäischen Kommission haben wir die untenstehende Anfrage erhalten die wir an Sie weitergeben möchten. Wenn Sie derzeit 3D Druckkapazitäten frei haben, melden Sie sich bitte nicht mehr (aktualisiert 2024).

Die Anfrage richtet sich vor allem an Unternehmen, die größere Kapazitäten zur Verfügung stellen können. Für kleinere Unternehmen und Einzelpersonen, die ebenfalls gerne helfen wollen, finden hier eine großartige Initiative, die Organisationen und Maker deutschlandweit zusammenbringt: https://www.makervsvirus.org/de/

Wie Sie mit Ihrem Beitrag aus dem 3D-Drucker Leben retten können, zeigt dieses Beispiel aus Italien: https://www.3dprintingmedia.network/covid-19-3d-printed-valve-for-reanimation-device/

„There is an urgent need for masks (see also open source for printing masks) and 25.000 ventilators are needed for respirators, they can be 3D printed, see good example below. You might have these fablabs in your clusters which could be activated to work directly with the hospitals. Or to go on production, if so please let me know and we need to see how we can support this.”

Link zur oben angesprochenen Maske: https://www.opensourcemask.com

Hier finden Sie weitere Informationen zu den medizinischen Standards und Anforderungen (PDF).

* Possible exception:

In duly justified cases, the competent authorities of Member States may decide, within their territory, to authorise the placing on the market and putting into service of devices for which the relevant EU conformity assessment procedure(s) laid down in Directive 93/42/EEC on medical devices have not been carried out and the use of which is in the interest of protection of health.

Tenderers may therefore consider the submission of a separate tender bid for such devices, in particular where they can demonstrate, at the time of submission, that the concerned devices have been authorised in accordance with the conformity assessment procedures established under the national laws of at least one other third country.

Tenderers should note that it is the prerogative of each Member State to decide whether the placing on the market and putting into service of devices referred to above may be authorised on duly justified grounds.

Lot 2 – Ventilators II – invasive

Ventilators under this lot comply with the following minimum quality requirements: