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Two Medical

Company · Portugal

not in the EU Transparency RegisterThis organization files on consultations without a register number, so its record here is built from its filings alone. Register facts (staff, costs, accreditations) are not available for it.

3
positions filed
in the 665 files tracked
1
legislative file
of 665 tracked
0
with a full position paper
attached to a submission

Counts here are a floor, never a total: they cover the 665 consultation files tracked so far (57,774 submissions, mostly 2021–26), so an organization's real filing history is larger, not smaller.

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Their record over time

Two Medical filed 3 positions on 1 Oct 2025, across 1 of the 665 legislative files tracked here.

What they argued

Simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and support of the European Medicines Agency for the expert panels on medical devices and the list of Union harmonisation legislationfiled 1 Oct 2025source

This contribution aims to propose the explicit inclusion of dental bleaching agents with concentrations above 6 % hydrogen peroxide (or equivalent compounds that release hydrogen peroxide) in medical devices under Regulation (EU) 2017/745 (MDR) in the context of the ongoing targeted review.

Filed in Portuguese · English published by the European Commission

Simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and support of the European Medicines Agency for the expert panels on medical devices and the list of Union harmonisation legislationfiled 1 Oct 2025source

This contribution aims to propose the explicit inclusion of dental bleaching agents with concentrations above 6 % hydrogen peroxide (or equivalent compounds that release hydrogen peroxide) in medical devices under Regulation (EU) 2017/745 (MDR) in the context of the ongoing targeted review.

Filed in Portuguese · English published by the European Commission

Simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and support of the European Medicines Agency for the expert panels on medical devices and the list of Union harmonisation legislationfiled 1 Oct 2025source

This contribution aims to propose the explicit inclusion of dental bleaching agents with concentrations above 6 % hydrogen peroxide (or equivalent compounds that release hydrogen peroxide) in medical devices under Regulation (EU) 2017/745 (MDR) in the context of the ongoing targeted review.

Filed in Portuguese · English published by the European Commission

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Quotes are verbatim from submissions published by the European Commission, trimmed to their opening passage and never summarized by a model. Organizations only, never individuals. Reused under Commission Decision 2011/833/EU; the European Commission is not liable for this reuse.