FAQEU

RoHS FAQ Lead, Mercury, and Cadmium Exemptions

EU RoHS restricts lead and mercury to 0.1% by weight and cadmium to 0.01% by weight in each homogeneous material unless a specific Annex III or Annex IV exemption covers the application.

Use this FAQ to document the exact exemption entry, product category, material use, expiry or renewal status, and evidence package behind the decision.

Author
Sorena AI
Published
May 9, 2026
Updated
May 9, 2026
Questions
5

Structured answer sets in this page tree.

Primary sources
4

Cited legal and guidance references.

Publication metadata
Sorena AI
Published May 9, 2026
Updated May 9, 2026
Overview

Document a RoHS exemption for lead, mercury, or cadmium by tying it to the exact Annex III or Annex IV entry, the restricted substance, the homogeneous material or component application, the EEE category, the concentration or amount limit in the entry, the expiry or renewal status, and the supplier or test evidence that supports the finished product's technical documentation.

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5 of 5 questions
Question 1

How should RoHS exemptions for lead, mercury, and cadmium be documented?

Start from the restriction, then document the exception. Annex II lists lead and mercury at 0.1% by weight in homogeneous materials and cadmium at 0.01%. Article 4 says those limits do not apply to applications listed in Annex III or Annex IV, so an exemption record must prove that the product's use matches a specific listed application.

Avoid documenting exemptions as broad product permissions. The Commission RoHS FAQ explains that exemptions are granted for specific substances used in specific applications, not for a company or for a whole piece of EEE. A useful record therefore identifies the substance, material, component, product category, and Annex wording that supports the exception.

Do not make an unsourced current-status table for lead, mercury, or cadmium exemptions. Annex entries are technical and time-limited, and many include category-specific expiry dates, scope limits, spare-parts wording, amount limits, or renewal effects. Keep the official source URL and the date you checked it with the exemption record.

  • Record the Annex III or Annex IV entry number and quote or summarize the exact application wording used for the decision.
  • Map the entry to the EEE category, product model, part number, material, supplier, revision, and homogeneous material where the restricted substance appears.
  • Capture the measured or declared concentration, or the per-lamp, per-display, or application-specific amount limit where the Annex entry uses one.
  • State the expiry date, renewal application status, pending Commission decision status, or spare-parts condition that affects continued reliance.
  • Keep supplier declarations, material declarations, risk assessment, test reports where used, and EN IEC 63000 technical documentation together with the exemption rationale.
Citations
Question 2

What to capture for lead, mercury, and cadmium entries

The documentation fields differ because the Annex entries differ. Mercury lamp exemptions often use per-lamp or per-burner milligram limits and specific lamp technologies. Lead entries include alloys, solders, glasses, ceramics, coatings, bearings, and application-specific electronic components. Cadmium entries include electrical contacts, optical or filter glass uses, printing inks, thick film pastes, quantum dots, and specialized measurement or monitoring uses.

Use those examples as a cue for record structure, not as a substitute for checking the exact entry. The support file should be precise enough that an auditor can compare the product facts with the Annex wording without asking engineering to reconstruct the design history.

  • For mercury lamp exemptions, record the lamp type, wattage or technology condition, per-lamp or per-burner mercury limit, and expiry date stated in the Annex entry.
  • For lead alloy and solder exemptions, record the alloy, solder, component, voltage, application, product category, and any percentage threshold or excluded application.
  • For cadmium exemptions, record the compound, contact, glass, ink, paste, quantum-dot, measurement, or monitoring application and the category or amount condition stated in the entry.
  • For Annex IV medical-device and monitoring-equipment exemptions, confirm that the product is actually in the category covered by Annex IV before relying on the entry.
  • When an entry has expired, document whether Article 4 spare-parts wording, a renewal application, or a Commission decision affects the specific product.
Citations
Question 3

Evidence to keep in the RoHS technical file

RoHS documentation should connect the exemption decision to the conformity assessment file. Directive 2011/65/EU requires manufacturers to draw up technical documentation, carry out the relevant conformity assessment procedure, draw up the EU declaration of conformity, affix CE marking, and keep the technical documentation and EU declaration of conformity for 10 years after the EEE has been placed on the market.

Commission Implementing Decision (EU) 2020/659 identifies EN IEC 63000:2018 as the harmonised standard for technical documentation used to assess materials, components, and EEE against RoHS restricted-substance requirements. Use that structure to keep supplier declarations, material declarations, test reports where needed, exemption mapping, and change-control evidence aligned.

  • BOM and material breakdown showing where lead, mercury, or cadmium appears.
  • Supplier declaration or material declaration tied to the exact part number, material, revision, and restricted substance.
  • Test report or engineering assessment where supplier data is incomplete, high risk, or inconsistent with the product design.
  • Exemption register entry with source URL, Annex entry, EEE category, application wording, limit, expiry, owner, and review date.
  • EU declaration of conformity and technical documentation references showing how the exemption supports the Article 4 compliance conclusion.
Citations
Recommended next step

Document exemption evidence before relying on it

Review the Annex entry, material facts, supplier evidence, expiry status, and technical-file records behind lead, mercury, or cadmium use in your EEE.

Question 4

Expiry, renewal, and change-control checks

Exemption evidence should not stop at the date the product launched. Article 5 says exemptions have validity periods, may be renewed, and can be deleted when the conditions for inclusion are no longer fulfilled. A renewal application must be made no later than 18 months before the exemption expires, and an existing exemption remains valid until the Commission decides on that renewal application.

The Commission implementation page states that RoHS exemptions are limited in time and reassessed regularly, considering substitute availability, practicability and reliability, environmental, health and consumer safety impacts, socioeconomic impact, and potential adverse impacts on innovation. It also states that a RoHS exemption decision currently takes 18 to 24 months from the application date.

  • Review the exemption when the Annex entry changes, the expiry date approaches, or a renewal or revocation decision is published.
  • Review the record after product redesign, supplier change, material change, solder or coating change, lamp change, or category change.
  • If a renewal request is pending, keep the evidence for that status with the exemption record instead of relying on an informal note.
  • If the exemption is rejected, revoked, or no longer matches the product, open a substitution, redesign, withdrawal, or customer-impact decision before relying on further EU market placement.
  • Do not assume spare-parts provisions apply unless the product and exemption facts match Article 4 wording for the specific case.
Citations
Question 5

Common mistakes when documenting these exemptions

The most common mistake is treating the word "exempt" as the conclusion instead of documenting the legal and technical match. Lead, mercury, and cadmium exemptions are narrow, and the same substance can appear in multiple entries with different applications, categories, concentration limits, amount limits, and dates.

Another weak pattern is relying on a supplier's generic RoHS statement after a material, category, or Annex entry changes. A defensible exemption record should survive supplier changes, market-surveillance questions, customer audits, and future product changes.

  • Do not cite an Annex entry without checking that the material and application match the entry wording.
  • Do not average lead, mercury, or cadmium across the finished EEE; the default limits are homogeneous-material limits unless a valid exemption applies.
  • Do not reuse a lead exemption for cadmium or mercury, or reuse an Annex III exemption where Annex IV category specificity is required.
  • Do not omit expiry, renewal, or pending-decision status when the entry includes date-sensitive wording.
  • Do not put local source reference filenames, private working notes, or stale non-HTTPS URLs in public source fields.
Citations
Primary sources

References and citations

ec.europa.eu
Referenced sections
  • Commission FAQ explaining that exemptions are not granted for a company or whole EEE and that material limits are applied individually.
"not for the whole EEE, nor for a company"
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