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Textual twins

Medical Devices Regulation Art. 92 and IVDR Art. 87 where the texts differ

textually similar (0.968) · paired on the Medical Devices Regulation text of 19 July 2026 and the IVDR text of 10 January 2025 · headings different

Medical Devices Regulation Art. 92 and IVDR Art. 87 are textually similar: their words match at a ratio of 0.968, 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. 92IVDR Art. 87
1

Article 92 Electronic system on vigilance and on

Article 87 Electronic system on vigilance and post-market

2

92 Electronic system on vigilance and on post-market surveillance 1. The Commission shall,

87 Electronic system on vigilance and post-market surveillance 1. The Commission shall,

3

and process the following information: (a) the reports by manufacturers on serious incidents

and process the following information: (a) reports by manufacturers on serious incidents

4

corrective actions referred to in Article 87(1) and Article 89(5); (b) the periodic

corrective actions referred to in Article 82(1) and Article 84(5); (b) the periodic

5

to in Article 87(1) and Article 89(5); (b) the periodic summary reports by

to in Article 82(1) and Article 84(5); (b) the periodic summary reports by

6

by manufacturers referred to in Article 87(9); (c) the reports by manufacturers on

by manufacturers referred to in Article 82(9); (c) the reports by manufacturers on

7

on trends referred to in Article 88; (d) the PSURs referred to in

on trends referred to in Article 83; (d) the PSURs referred to in

8

the PSURs referred to in Article 86; (e) the field safety notices by

the PSURs referred to in Article 81; (e) the field safety notices by

9

by manufacturers referred to in Article 89(8); (f) the information to be exchanged

by manufacturers referred to in Article 84(8); (f) the information to be exchanged

10

the Commission in accordance with Article 89(7) and (9). That electronic system shall

the Commission in accordance with Article 84(7) and (9). That electronic system shall

11

a certificate in accordance with Article 53. 3. The Commission shall ensure that

a certificate in accordance with Article 49. 3. The Commission shall ensure that

12

to in point (a) of Article 87(1) shall be automatically transmitted, upon receipt,

to in point (a) of Article 82(1), shall be automatically transmitted, upon receipt,

7 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.