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Daily: snapshots/state/report [skip ci]
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last_diff.txt

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### Issue #4
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**Page:** [https://health.ec.europa.eu/medical-devices-sector/new-regulations_en](https://health.ec.europa.eu/medical-devices-sector/new-regulations_en)
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**Changes:** Text & Links
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**Full text diff:**
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```
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--- Issue #4 (old)
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+++ Issue #4 (new)
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@@ -290,7 +290,9 @@
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2025
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Delegated Regulation 2025/1920 – UDI assignment for spectacle frames and lenses
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2023
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-Delegated Regulation 2023/2197 – UDI assignment for contact lenses and application-date amendment
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+Delegated Regulation 2023/2197 – UDI assignment for contact lenses
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+and
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+Commission Delegated Regulation (EU) 2025/788 amending the date of application
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Delegated Regulation 2023/502 – frequency of complete re-assessments of notified bodies (C/2022/8640)
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Delegated Regulation 2023/503 – frequency of complete re-assessments of notified bodies (C/2022/8649)
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2022
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@@ -422,7 +424,7 @@
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Accessibility
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-{"utility":"piwik","siteID":"f573665d-3da7-4fad-8552-baccf7ee0b46","sitePath":["health.ec.europa.eu"],"instance":"ec","dimensions":[{"id":3,"value":"Page"},{"id":4,"value":"medical-device"},{"id":5,"value":"Directorate-General-for-Health-and-Food-Safety"},{"id":6,"value":"New Regulations"},{"id":7,"value":"fafbce50-281c-4195-a2d7-22c9fc22c58f"},{"id":8,"value":"EC - STANDARDISED"},{"id":9,"value":"medical-device health-policy"},{"id":10,"value":"Default landing page"},{"id":12,"value":"503"}]}
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+{"utility":"piwik","siteID":"f573665d-3da7-4fad-8552-baccf7ee0b46","sitePath":["health.ec.europa.eu"],"instance":"ec","dimensions":[{"id":3,"value":"Page"},{"id":4,"value":"medical-device"},{"id":5,"value":"Directorate-General-for-Health-and-Food-Safety"},{"id":6,"value":"New Regulations"},{"id":7,"value":"fafbce50-281c-4195-a2d7-22c9fc22c58f"},{"id":8,"value":"EC - STANDARDISED"},{"id":9,"value":"medical-device health-policy"},{"id":10,"value":"Default landing page"},{"id":12,"value":"505"}]}
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{"utility":"cck"}
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```
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**Added links (all):**
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- https://eur-lex.europa.eu/eli/reg_del/2025/788/oj
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# ReguWatch — Daily Summary
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Date (UTC): 2026-02-01
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state/last_run.json

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{
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"https://www.fda.gov/medical-devices": "2026-01-31T05:39:02.784979Z",
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"https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/guidance-documents-medical-devices-and-radiation-emitting-products": "2026-01-31T05:39:02.830939Z",
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"https://health.ec.europa.eu/medical-devices-sector/new-regulations/guidance-mdcg-endorsed-documents-and-other-guidance_en": "2026-01-31T05:39:03.576109Z",
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"https://health.ec.europa.eu/medical-devices-sector/new-regulations_en": "2026-01-31T05:39:03.779092Z",
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"https://health.ec.europa.eu/medical-devices-sector/directives_en": "2026-01-31T05:39:03.851934Z",
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"https://health.ec.europa.eu/medical-devices-sector/vitro-diagnostics_en": "2026-01-31T05:39:05.544977Z",
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"https://health.ec.europa.eu/medical-devices-sector/eudamed_en": "2026-01-31T05:39:05.778016Z",
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"https://health.ec.europa.eu/medical-devices-sector/guidance-and-useful-information_en": "2026-01-31T05:39:05.978893Z",
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"https://health.ec.europa.eu/medical-devices-sector/coordination-and-governance_en": "2026-01-31T05:39:06.194289Z",
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"https://www.fda.gov/medical-devices": "2026-02-01T05:59:27.840721Z",
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"https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/guidance-documents-medical-devices-and-radiation-emitting-products": "2026-02-01T05:59:27.986159Z",
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"https://health.ec.europa.eu/medical-devices-sector/new-regulations/guidance-mdcg-endorsed-documents-and-other-guidance_en": "2026-02-01T05:59:28.468342Z",
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"https://health.ec.europa.eu/medical-devices-sector/new-regulations_en": "2026-02-01T05:59:29.011414Z",
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"https://health.ec.europa.eu/medical-devices-sector/directives_en": "2026-02-01T05:59:29.573091Z",
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"https://health.ec.europa.eu/medical-devices-sector/vitro-diagnostics_en": "2026-02-01T05:59:29.751967Z",
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"https://health.ec.europa.eu/medical-devices-sector/eudamed_en": "2026-02-01T05:59:31.404857Z",
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"https://health.ec.europa.eu/medical-devices-sector/guidance-and-useful-information_en": "2026-02-01T05:59:31.639316Z",
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"https://health.ec.europa.eu/medical-devices-sector/coordination-and-governance_en": "2026-02-01T05:59:32.166886Z",
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"https://webstore.iec.ch/en/just-published/": "2025-10-06T18:39:40.904557Z",
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"https://www.iso.org/insights/standards-world": "2026-01-31T05:39:06.572064Z",
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"https://www.iso.org/insights/standards-world": "2026-02-01T05:59:32.540454Z",
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"https://www.fda.gov/news-events/fda-newsroom/press-announcements": "2025-10-06T18:39:41.201680Z",
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"https://www.bbc.com/news": "2025-10-06T18:39:41.381647Z",
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"https://webstore.iec.ch/en/just-published/](https://webstore.iec.ch/en/just-published/)": "2025-10-06T18:39:42.027217Z",
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"https://www.fda.gov/news-events/fda-newsroom": "2026-01-31T05:39:06.636448Z"
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"https://www.fda.gov/news-events/fda-newsroom": "2026-02-01T05:59:32.689060Z"
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}

state/monthly_counters.json

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{
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"month": "2026-01",
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"checks": 341,
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"month": "2026-02",
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"checks": 11,
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"webhooks": 0
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}

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