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Omnibus update (7 May 2026): Annex III high-risk provisionally shifted from 2 Aug 2026 to 2 Dec 2027. Art. 50 transparency (chatbots, deepfakes, emotion, biometric) still 2 Aug 2026. Art. 4 / Art. 5 / GPAI live now. Details.

Notified body capacity — Act now

Annex III high-risk enforcement is provisionally 2 December 2027 under the Digital Omnibus political agreement of 7 May 2026 (was 2 August 2026). Notified body assessments for high-risk AI systems requiring third-party conformity assessment (Annex III(1) remote biometric identification, plus Annex I product-embedded systems) typically take 9–18 months.

The Omnibus delay does not remove the queue: if anything the deferral has compressed the window in which providers must engage with NBs that are still being designated. Initiate contact now.

Recommended action: contact 2–3 candidate bodies now to obtain availability and indicative timelines. EU capacity is expected to be constrained well into 2027.

Free Tool · Art. 33

Notified Body Finder

Candidate EU notified bodies for AI Act conformity assessment by sector and Annex III category. Illustrative reference only — every entry must be verified in NANDO before contracting.

Why this matters

When Annex VII third-party conformity assessment is required, you must engage a notified body designated under the AI Act for your specific Annex III category. The wrong body invalidates the assessment. Bodies are listed in the Commission's NANDO database.

How to use it
  1. 1Select your Annex III category.
  2. 2Review the list of currently designated notified bodies for that category.
  3. 3Contact shortlisted bodies early — lead times and capacity vary.
  4. 4Record your choice and contract details in the technical file.
Legal basis
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When is a notified body required?

1. Biometric identification systems

Remote biometric identification systems used in publicly accessible spaces by law enforcement require mandatory third-party assessment under Art. 43(1) and Annex VII.

2. Annex I product safety components

AI systems embedded as safety components in Annex I products (e.g. medical devices, machinery) where the Annex I legislation itself requires third-party conformity assessment (e.g. Class IIa/IIb/III medical devices under MDR).

All other high-risk AI systems (Annex III, non-biometric) may use internal-control self-assessment under Annex VI. Check your assessment path →

As of May 2026, no notified body has been formally designated under Art. 29 in the public NANDO register for AI Act high-risk conformity assessment. The candidates below are illustrative and should be verified in NANDO before contracting.

Reference only. Always verify current accreditation status on the European Commission's NANDO (New Approach Notified and Designated Organisations) database at ec.europa.eu/growth/tools-databases/nando/. EU AI Act notified body designations under Art. 33 are being processed by Member State authorities; bodies in this list have existing sector accreditations and have publicly signalled an intention to seek AI Act notification.

Filters narrow the illustrative list. Annex III filter is keyed to each body's adjacent sector competence, not to a confirmed AI Act designation.

8 candidate bodies found · illustrative

NANDO Database (official)

TÜV SÜD AG

Illustrative — verify in NANDO
Existing NB ID: 0123 (under sector legislation, not Art. 29)Countries: Germany
Annex I sectorsMedical DevicesMachineryCritical Infrastructure
Annex III adjacency1 — Biometrics2 — Critical infrastructure
Visit website

TÜV Rheinland

Illustrative — verify in NANDO
Existing NB ID: 0035 (under sector legislation, not Art. 29)Countries: Germany
Annex I sectorsMedical DevicesMachineryCybersecurity
Annex III adjacency1 — Biometrics2 — Critical infrastructure
Visit website

Bureau Veritas

Illustrative — verify in NANDO
Existing NB ID: 0041 (under sector legislation, not Art. 29)Countries: France
Annex I sectorsMedical DevicesGeneral Product Safety
Annex III adjacency1 — Biometrics5(a) — Essential services
Visit website

SGS Belgium NV

Illustrative — verify in NANDO
Existing NB ID: 1639 (under sector legislation, not Art. 29)Countries: Belgium
Annex I sectorsGeneral Product SafetyMedical Devices
Annex III adjacency1 — Biometrics

Lloyd's Register EMEA

Illustrative — verify in NANDO
Existing NB ID: 0038 (under sector legislation, not Art. 29)Countries: Netherlands, UK (NB)
Annex I sectorsCritical InfrastructureMaritime
Annex III adjacency2 — Critical infrastructure
Visit website

DEKRA Certification

Illustrative — verify in NANDO
Existing NB ID: 0905 (under sector legislation, not Art. 29)Countries: Germany, Spain
Annex I sectorsAutomotiveMachinery
Annex III adjacency2 — Critical infrastructure
Visit website

Intertek

Illustrative — verify in NANDO
Existing NB ID: 1725 (under sector legislation, not Art. 29)Countries: Netherlands
Annex I sectorsGeneral Product SafetyElectronics
Annex III adjacency1 — Biometrics
Visit website

DNV

Illustrative — verify in NANDO
Existing NB ID: 0575 (under sector legislation, not Art. 29)Countries: Norway, Netherlands
Annex I sectorsMaritimeEnergyCritical Infrastructure
Annex III adjacency2 — Critical infrastructure
Visit website

Notified body information last reviewed May 2026. The authoritative source is the EU NANDO database. Designation status changes; always verify before contracting.

Note on AI Act notified body designation: Art. 29 designations are made by Member State national accreditation bodies (NABs) under Art. 33 and published in NANDO by the Commission. As of May 2026 none have been published specifically for AI Act high-risk assessment. Bodies with existing MDR/IVDR, Machinery Regulation, or radio-equipment accreditation are expected to seek AI Act notification for overlapping sectors. Engage candidate bodies early — capacity is expected to be constrained well into 2027 even with the Digital Omnibus enforcement deferral to 2 December 2027.