Directive 2014/53/EU · Del. Reg. 2022/30Generate my documentation — €99
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Module A or Notified Body? The conformity route depends on how you apply EN 18031. The technical documentation is required either way — and REDCheck generates it for both.

Art. 17 of Directive 2014/53/EU defines three conformity assessment routes for the cybersecurity requirements of Art. 3(3). If you fully apply the harmonised standards EN 18031-1, -2 and -3 (where applicable), Art. 17(3)(a) allows self-declaration via Module A (Annex II) — no Notified Body needed. If you partially apply or do not apply them, Art. 17(4) requires Module B+C (Annex III — EU-type examination) or Module H (Annex IV — full quality assurance) with Notified Body involvement. In BOTH cases, Art. 21 requires the manufacturer to prepare technical documentation under Annex V BEFORE any conformity route can be followed. REDCheck generates this prerequisite documentation. 30 minutes. €99 per product.

Generate my RED documentation — €99Free: does my product need RED cybersecurity documentation?

€99 one-time payment · 5 PDF documents in ZIP · 30 minutes · 100% in your browser

Directive 2014/53/EU · Art. 3(3)(d)(e)(f) · Art. 21 + Annex V · Art. 18 + Annex VI · Art. 10(9) + Annex VII · Delegated Reg. (EU) 2022/30 · EN 18031-1, -2, -3

Module A vs Notified Body: the numbers

The choice between Module A and a Notified Body is not about preference — it is determined by Art. 17 based on how you apply the harmonised standards.

Module A
Self-declaration. Internal production control (Annex II). Available when EN 18031 is FULLY applied. Art. 17(3)(a). Cost: €0 for the conformity route itself.
Module B+C or H
Notified Body involvement. Required when EN 18031 is NOT fully applied. Art. 17(4). Cost: €5,000–20,000 per product model.
Art. 21
Technical documentation required for BOTH routes. REDCheck generates it: €99 per product.

How the conformity route decision works

The flowchart is embedded in Art. 17. REDCheck does not choose the route for you — it generates the documentation that both routes require as input.

1
Identify applicable essential requirements
Art. 3(3)(d): internet-connected? Art. 3(3)(e): processes personal data or falls in childcare/toy/wearable category? Art. 3(3)(f): enables money transfer?
2
Assess EN 18031 application
Do you fully apply all requirements of the applicable EN 18031 parts? Fully = every applicable requirement implemented, including those under Implementing Decision (EU) 2025/138 restrictions.
3
If FULLY applied → Module A
Art. 17(3)(a): internal production control (Annex II). You self-declare conformity. No Notified Body. You sign the EU declaration of conformity. You affix CE marking.
4
If NOT fully applied → Module B+C or H
Art. 17(4): EU-type examination (Annex III) or full quality assurance (Annex IV). A Notified Body examines your technical design and issues a certificate. The technical documentation under Art. 21 is the input to this examination.
5
Generate technical documentation
Regardless of route: Art. 21 requires complete documentation under Annex V. For Module A, it IS your evidence of conformity. For Module B+C or H, it is the dossier you submit to the Notified Body.
6
Download ZIP
5 PDF documents. Whether you self-declare or submit to a Notified Body, the documentation package is the same.

Three mistakes manufacturers make about conformity routes

COMMON ERROR

"Module A means no documentation is needed"

The opposite. Module A (Annex II) paragraph 2 states: 'The manufacturer shall establish the technical documentation in accordance with Article 21.' Module A is self-declaration, NOT self-exemption. The difference is who reviews: in Module A, you self-assess. In Module B+C, a Notified Body examines. But the documentation requirement is identical.

COMMON ERROR

"We mostly apply EN 18031 — that's close enough for Module A"

'Mostly' is not 'fully.' Art. 17(3)(a) requires the manufacturer to have 'applied harmonised standards the references of which have been published in the OJEU.' Partial application triggers Art. 17(4), which requires Notified Body involvement. There is no middle ground. One unmet requirement moves you from Module A to Module B+C or H.

COMMON ERROR

"A Notified Body will produce the documentation for us"

A Notified Body EXAMINES your documentation — it does not PRODUCE it. Art. 34(1): Notified Bodies carry out conformity assessments 'in accordance with the conformity assessment procedures provided for in Annexes III and IV.' The manufacturer must submit complete technical documentation for examination (Annex III, Module B, paragraph 3(c)). If your documentation is incomplete, the Notified Body returns the file. REDCheck generates the documentation you submit.

What's in the ZIP

5 PDF documents generated from your product data. Each cites the exact article of Directive 2014/53/EU that it covers.

1

Product Classification

Art. 1, Del. Reg. (EU) 2022/30 + Art. 3(3), Dir. 2014/53/EU.

2

Cybersecurity Technical Documentation

Art. 21 + Annex V. Requirement-by-requirement documentation.

3

Risk Assessment

Arts. 3(3)(d) and (e). Structured risk table.

4

EU Declaration of Conformity

Art. 18 + Annex VI.

5

Simplified Declaration + Label

Art. 10(9) + Annex VII.

Look before you buy — Download sample dossier (PDF, fictitious product) — Real structure, real articles, real format. Fictitious data.

Generated from your data, in your browser. No product data leaves your computer.

What you pay

🧾 NOTIFIED BODY (MODULE B+C)
€5,000–20,000
Per product model. 2–6 months. Assessment + certificate. Required ONLY if EN 18031 not fully applied.
✓ REDCHECK
€99
Technical documentation for EITHER route. 30 minutes. Required for Module A AND Module B+C.

Technical documentation and third-party testing: two layers

● LAYER 1

Cybersecurity technical documentation (Annex V)

5 PDF documents. 30 min. €99 per product. Maps your EN 18031 assessment to the Annex V structure. This is what Art. 21 requires BEFORE your product can bear CE marking — regardless of conformity route.

∅ LAYER 2

Conformity assessment route

If you fully apply EN 18031, Art. 16 grants presumption of conformity → Module A self-declaration (Annex II) without Notified Body. If partially applied or not applied: Art. 17(4) requires Module B+C (Annex III) or Module H (Annex IV) with Notified Body. REDCheck generates the Layer 1 documentation that is a prerequisite for EITHER route.

We do not assess your product. We do not interpret EN 18031. We structure the documentation that Art. 21 requires based on YOUR assessment of YOUR product.

What happens without documentation

Art. 46 of Directive 2014/53/EU requires Member States to establish penalties.

🇪🇺
Market withdrawal
Immediate

Art. 40 of Directive 2014/53/EU. Market surveillance can require withdrawal across all 27 Member States.

🇩🇪
Germany — Produktsicherheitsgesetz
€3,000–€30,000

Administrative fines under §19. Up to 1 year imprisonment under §20.

📋
Module A challenged by market surveillance
Re-assessment at manufacturer's expense

Art. 21(4): if technical documentation is insufficient, the authority can require testing by an acceptable body AT THE MANUFACTURER'S EXPENSE. A weak Module A self-declaration with incomplete documentation invites scrutiny.

Documentation options for either conformity route

AlternativeCostWhat you get
Notified Body (full service)€5,000–20,000 per modelAssessment + documentation + certificate. Only needed if EN 18031 not fully applied.
EU cybersecurity consultancy€3,000–15,000 per modelCustom documentation. May or may not follow Annex V structure.
Draft documentation internally€0 (your time)No template. Annex V has 9 required elements. Risk of incomplete submission.
REDCheck€99Annex V documentation for Module A or input to Notified Body. 30 min.

Documenting more than one product model?

Professional Pack: €999 for 70 generations.

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What REDCheck guarantees and what it does not

REDCheck generates a document structured under Art. 21 and Annex V of Directive 2014/53/EU based on the information you enter. The truthfulness, accuracy and completeness of that information is your responsibility as manufacturer of the radio equipment.

We guarantee that the document structure follows Art. 21 and Annex V of Directive 2014/53/EU and that the legal references cited are correct as of the latest verification date. We do not guarantee that a specific document will be accepted by a market surveillance authority in a specific case, nor by a commercial buyer in a procurement process.

REDCheck is not legal advice. For specific situations, consult a lawyer or specialised regulatory consultancy.

Frequently asked questions — Module A vs Notified Body

How do I know if I 'fully apply' EN 18031?
You fully apply EN 18031 when every applicable requirement in the relevant parts (EN 18031-1, -2, -3) is implemented in your product as specified, AND the implementation does not fall under any restriction listed in Implementing Decision (EU) 2025/138. If even one applicable requirement is 'partially implemented' or 'not applicable due to design choice,' you do not fully apply and Art. 17(4) directs you to Module B+C or H.
Can I start with Module A and switch to Notified Body later?
Yes, but it is better to decide before placing the product on the market. If you self-declare under Module A and a market surveillance authority later determines that EN 18031 was not fully applied, Art. 21(4) allows them to order testing at your expense. The safer path: assess your EN 18031 application status honestly, use the correct route from the start, and document everything.
Does REDCheck tell me which route I need?
The product classification step identifies which EN 18031 parts apply and asks you to assess your implementation status. If you indicate full application, the documentation is formatted for Module A. If partial, the documentation notes that Art. 17(4) applies and the EU declaration of conformity is pre-formatted to reference a Notified Body certificate. REDCheck structures — it does not decide for you.
What happens when the CRA replaces the RED cybersecurity requirements?
Delegated Regulation (EU) 2022/30 will be repealed with effect from 11 December 2027, when the Cyber Resilience Act — Regulation (EU) 2024/2847 — enters full application. REDCheck covers the window from 1 August 2025 to 11 December 2027. For CRA documentation from that date, SolidwareTools offers CRACheck.
Is it a subscription?
No. One-time payment. Each license includes a 30-day editing window and up to 10 regenerations. The 5 PDF documents you download are yours permanently.
Can I request a refund?
Under Art. 16(m) of Directive (EU) 2011/83 on consumer rights, by activating the license you give express consent to the immediate generation of the digital content, waiving the 14-day right of withdrawal. Refunds are accepted only for reproducible technical failures reported to hello@solidwaretools.com within 14 days of purchase.
What if the regulation changes?
If Directive 2014/53/EU, Delegated Regulation (EU) 2022/30 or the EN 18031 standards change during your license validity period, you can regenerate the documents with the updated version of the generator at no additional cost.
⚠️ Important notice: REDCheck is a documentary self-assessment tool, not legal advice or a third-party audit. The document is generated from the data you enter. The accuracy of the data is your responsibility under Art. 10(1) of Directive 2014/53/EU. REDCheck does not replace a conformity assessment by a Notified Body where required under Art. 17(4) of the Directive.

Module A or Notified Body — the documentation is the same. Generate it in 30 minutes.

Five PDF documents. Art. 21 and Annex V fully structured. Directive 2014/53/EU. Your product data never leaves your computer.

€99 per product
One-time payment · No subscription · 30 minutes · 10 regenerations · 30-day editing window · Professional Pack: €999
Generate my RED documentation — €99
✓ Last regulatory check: 6 May 2026 · No substantive changes detected · View history