PhaRegistrum · Originally published on 09/06/2026
Portuguese Order No. 206/2026/1, in force since 5 May, approves the list of single-use medical devices whose reprocessing is expressly prohibited, in line with Regulation (EU) 2017/745 (MDR).
The prohibition includes:
- Implantable devices.
- Devices that emit radiation.
- Devices used in invasive central nervous system or ophthalmic procedures.
- Devices with non-replaceable batteries or internal data storage.
Failure to comply may create legal risks and risks to patient safety.
PhaRegistrum supports companies in adapting to new medical device regulatory requirements. Contact us.
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