Reg (EU) 2024/2847Generate dossier — €149
LIVE — Enforcement tracker · Deadline dashboard · Transposition status — Updated weekly from EUR-Lex, Safety Gate, OEIL & 12 official sourcesView regulatory intelligence →

Annex III point 19 of Regulation (EU) 2024/2847 classifies "personal wearable products with a health monitoring purpose" as Important Class I — provided they are not medical devices under Regulation (EU) 2017/745. Your fitness tracker measures heart rate, blood oxygen and sleep patterns. It is not a medical device. It is Class I under CRA. CRACheck generates the Annex VII technical documentation.

A fitness tracker collects biometric data — heart rate, SpO2, movement patterns, sleep. This data is processed locally and transmitted to a companion app via Bluetooth. Annex I Part I point 1(c) requires protection of confidentiality of data. Annex III point 19 classifies health-monitoring wearables as Important Class I. If harmonised standards are not fully applied, conformity assessment by a notified body is required under Article 32.2. CRACheck generates 8 PDF documents per Annex VII. 15-25 minutes. €149. Browser-side.

Generate CRA dossier — €149Free: check your product classification

€149 one-time · 8-document ZIP · 15–25 minutes · Browser-side

Regulation (EU) 2024/2847 · Art. 31 + Annex VII · 8 documents · 100% browser-side

Key numbers

Class I
Health-monitoring wearables — Annex III point 19. Biometric data raises the cybersecurity classification.
Biometric data
Heart rate, SpO2, sleep. Annex I Part I point 1(c): confidentiality of data is mandatory.
€149
Per tracker model. Class I documentation ready for notified body review.

How CRACheck works

You enter your product data. CRACheck structures the documentation per Article 31 + Annex VII.

1
Confirm classification
Health-monitoring wearable, not a medical device. Annex III point 19. Class I.
2
Map biometric data flow
Sensors → local processing → Bluetooth → companion app → cloud (if applicable). Document each stage.
3
Generate CRA dossier
Enter your tracker's specifications into CRACheck. 15-25 minutes.
4
Engage notified body
If harmonised standards are not fully applied, submit documentation for Module B+C or Module H.
5
Update companion app disclosures
Annex II requires user information on data handling, support period and vulnerability reporting.
6
Deliver to EU channels
Amazon, fitness retailers and distributors receive your compliance documentation.

Common mistakes

ANNEX III.19

"Our fitness tracker is a consumer gadget — it is not regulated like medical devices"

Correct — your tracker is not a medical device. But that is precisely why it falls under CRA Annex III point 19: "personal wearable products with a health monitoring purpose to which Regulation (EU) 2017/745 does not apply." Being excluded from medical device regulation puts you inside CRA Class I.

ANNEX I, PART I, 1(c)

"Heart rate data is not sensitive — it is just a number"

Annex I Part I point 1(c) requires protection of confidentiality of stored, transmitted and processed data without distinction by data type. Heart rate patterns, sleep data and SpO2 readings are personal health data under GDPR and must be protected from unauthorized access under CRA.

ART. 13.5

"We use a third-party health sensor chip — the sensor vendor handles data security"

Article 13.5 requires due diligence on third-party components. The health sensor chip generates the biometric data, but your firmware processes, stores and transmits it. The security of the data pipeline is your responsibility.

What the ZIP contains

8 PDF documents generated from your data. Each cites the specific article of Regulation (EU) 2024/2847 it complies with.

1

Product Classifier

Class I confirmation per Annex III point 19. Biometric data raises the classification.

2

Technical Documentation

Art. 31 + Annex VII. Covers BLE connectivity, companion app data flow, biometric sensor integration.

3

Risk Assessment

Art. 13.2-13.3. Biometric data interception, unauthorized access to health records, firmware tampering.

4

User Information

Annex II. Data privacy, pairing security, factory reset.

5

Declaration of Conformity

Art. 28 + Annex V.

6

CVD Policy

Vulnerability disclosure for biometric data vulnerabilities.

7

Notification Template

Art. 14 ENISA notification. Art. 14(2): early warning within 24h, notification within 72h, final report within 14 days.

8

Obligations Calendar

CRA dates plus support period for the tracker.

See before you buy — Download sample dossier (PDF, fictional company) — Real structure, real articles, real format. Fictional data.

Generated from your data, in your browser. No data leaves your device.

What you pay

🧾 WEARABLE CERTIFICATION CONSULTANCY (EUROPE)
€8,000–€15,000
Per model. 3-5 months. Biometric data review.
✓ Last regulatory check: 1 May 2026 · No substantive changes detected · View history