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Textual twins

Medical Devices Regulation Art. 27 and IVDR Art. 24 where the texts differ

textually similar (0.939) · paired on the Medical Devices Regulation text of 19 July 2026 and the IVDR text of 10 January 2025 · headings the same

Medical Devices Regulation Art. 27 and IVDR Art. 24 are textually similar: their words match at a ratio of 0.939, where 1 is identical text. That says nothing about what either provision requires, or whether one should change because the other did.

Where the texts differ

Each passage is a differing span with up to 6 unchanged words either side, from the text as compared, spacing collapsed, and cut at 400 characters where it ends […]. It is an excerpt for reading where the two differ, not the verbatim text.

PassageMedical Devices Regulation Art. 27IVDR Art. 24
1

Article 27 Unique Device Identification system 1. The

Article 24 Unique Device Identification system 1. The

2

the traceability of devices, other than custom-made and investigational devices, and shall consist of the following:

the traceability of devices, other than devices for performance studies, and shall consist of the following:

3

down in paragraphs 8 and 9 of this Article respectively; (d) establishment of an electronic

down in paragraphs 8 and 9 respectively; (d) establishment of an electronic

4

database ) in accordance with Article 28. 2. The Commission shall, by means

database ) in accordance with Article 28 of Regulation (EU) 2017/745. 2. The Commission shall, by means

5

financial and administrative burdens for economic operators and health institutions. 3. Before placing

financial and administrative burdens for economic operators, health institutions and healthcare professionals. 3. Before placing

6

administrative burdens for economic operators and health institutions. 3. Before placing a device, other

for economic operators, health institutions and healthcare professionals. 3. Before placing a device, other

7

placing a device, other than a custom-made device, on the market, the manufacturer shall

placing a device, other than a device for performance study, on the market, the manufacturer shall

8

Before a device, other than a custom-made or investigational device, is placed on the market the

Before a device, other than a device for performance study, is placed on the market the

9

placed on the market the manufacturer shall ensure that the information referred to

placed on the market the manufacturer must ensure that the information referred to

10

to in Part B of Annex VI of the device in question are

to in Part B of Annex V of the device in question are

11

UDI database referred to in Article 28. 4. UDI carriers shall be placed

UDI database referred to in Article 25. 4. UDI carriers shall be placed

12

corrective actions in accordance with Article 87. 6. The Basic UDI-DI, as defined

corrective actions in accordance with Article 82. 6. The Basic UDI-DI, as defined

12 more passages not shown; read both on EUR-Lex.

Aligned sub-provisions

Medical Devices Regulation first, then IVDR, each with its word ratio.

Changes since the texts were paired

The record holds no change to either provision after the versions they were paired on.