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 unless a specific or exemption covers the application.

This FAQ helps 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
Oct 15, 2026
Overview

Document a for lead, mercury, or cadmium by tying it to the exact or entry, the restricted substance, the or component application, the 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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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 or , 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 . A useful record therefore identifies the substance, material, component, product category, and Annex wording that supports the exception.

Record the current legal status for each relied-on lead, mercury, or cadmium entry. Annex entries are technical and time-limited, and many include category-specific expiry dates, scope limits, spare-parts wording, amount limits, or renewal effects. Check the current consolidated Directive because amendments that applied from 1 July 2026 changed several lead entries. Keep the official source URL and the date checked with the exemption record.

  • Record the or entry number and quote or summarize the exact application wording used for the decision.
  • Map the entry to the category, product model, part number, material, supplier, revision, and 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, 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.

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

Document the exact or entry, restricted substance, or component application, category, product and supplier revision, concentration or amount limit, expiry or renewal status, evidence source, owner, and review trigger. The record should show why the specific application is exempt even though lead and mercury normally use a 0.1% homogeneous-material limit and cadmium normally uses a 0.01% limit.

Are RoHS exemptions for a whole product or company?

No. The Commission RoHS FAQ says exemptions are granted for specific substances used in specific applications, not for a company or the whole . A finished product can rely on an exemption only for the material or component application that actually matches the Annex wording.

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 record should distinguish an entry that is currently applicable, an existing entry kept valid by a submitted renewal request, and a new exemption request that has not yet been granted. Only the first two can support continued reliance.

  • 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 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 , or a Commission decision affects the specific product.
Question 3

Worked lighting example: verify a mercury claim against the official Annex

A supplier statement that says only 'mercury exempt for fluorescent lamp' cannot support release. contains technology-specific lamp entries, amount limits and dates rather than one lighting exemption. The reviewer must open the official consolidated Annex applicable to the planned release date, identify the exact entry and sub-entry, and match the marketed lamp to every condition in that wording.

For a replacement lamp, record whether it is single-capped or double-capped, its phosphor or other stated technology, rated power and lifetime conditions, the mercury amount per lamp or burner, the category and the entry's expiry or renewal status. Then check whether the lamp is sold as finished EEE, supplied with new EEE, or supplied as a spare part for older equipment. Those facts can change the applicable product and date analysis even when the lamp has the same base and shape.

  • Reject example: the supplier cites ' mercury exemption' but provides no entry number, lamp technology, mercury amount or current-status evidence. Mark the bill-of-materials (BOM) line unresolved; do not convert the claim into RoHS compliance.
  • Conditional acceptance example: the supplier identifies the exact entry applicable to the planned release date, lamp family, rated-power condition, measured or declared mercury amount and covered category. Link that evidence to the finished- BOM and set review triggers for lamp, supplier, mercury dose, category, amendment, renewal decision and expiry changes.
  • Legacy-service example: where an exemption used for original has expired, test the precise Article 4 spare-part wording and original placing-on-market date. An expired lamp entry does not create a general permission for new products or unrelated service lamps.
  • Industry record: lamp manufacturer and site, supplier part and revision, technology and power band, or per-lamp limit, test or declaration method, Annex entry, legal-status URL, date checked, affected stock-keeping units (SKUs), reviewer and next trigger.
Question 4

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 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 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, 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.
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 5

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 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 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 request is for a new exemption rather than renewal of an existing one, the product must meet RoHS until the Commission grants the exemption.
  • 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.
Question 6

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. Update the source and product match so a reviewer can check the conclusion after a supplier or product change, or during a customer or authority review.

  • 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 ; the default limits are homogeneous-material limits unless a valid exemption applies.
  • Do not reuse a lead exemption for cadmium or mercury. Use only for the categories and applications its entry covers; use only for its stated medical-device or monitoring-and-control application.
  • Do not omit expiry, renewal, or pending-decision status when the entry includes date-sensitive wording.
  • Keep the official Annex or delegated-act URL and date checked with the exemption record, and replace a superseded status source when the entry changes.
Primary sources

References and citations

eur-lex.europa.eu7 citations
Referenced sections
  • Binding consolidated RoHS source for Article 4, Annex II thresholds, Annex III and IV exemptions, Article 5 validity and renewal rules, technical documentation, CE marking, and EU declaration of conformity.
  • Binding consolidated RoHS source for Annex II limits, Article 4 exemptions, Annex III, Annex IV, technical documentation, CE marking, and EU declaration of conformity obligations.
  • Binding consolidated RoHS source for Annex III and Annex IV exemption entries covering lead, mercury, and cadmium applications.
Show 4 more
  • Binding consolidated text for technology-specific Annex III mercury lamp entries, amount conditions, category-sensitive dates, Article 4 spare-part treatment and Article 5 renewal rules.
  • Binding source for manufacturer duties, technical documentation, EU declaration of conformity, CE marking, and 10-year retention.
  • Binding source for Article 5 validity periods, renewal timing, pending-renewal validity, revocation, and spare-parts provisions.
  • Binding source for homogeneous-material limits, Annex III and IV exemption wording, and Article 5 deletion or renewal rules.
"Applications exempted from the restriction in Article 4(1)"
More quoted passages
"Paragraph 1 shall not apply to the applications listed in Annexes III and IV."
"Mercury in single capped (compact) fluorescent lamps"
"keep the technical documentation and the EU declaration of conformity for 10 years"
"An application for renewal of an exemption shall be made no later than 18 months before the exemption expires."
"where the conditions set out in point (a) are no longer fulfilled"
environment.ec.europa.eu7 citations
Referenced sections
  • Commission FAQ source for application-specific exemptions, homogeneous-material threshold explanations, technical documentation context, and Annex III versus Annex IV roles.
  • Commission FAQ explaining that RoHS exemptions are application-specific and that homogeneous-material limits apply individually.
  • Commission FAQ explaining exemption specificity and the individual homogeneous-material threshold concept.
Show 4 more
  • Non-binding guidance supporting application-specific exemption and homogeneous-material evidence rather than company-wide or whole-product claims.
  • Commission FAQ context for technical documentation and homogeneous-material compliance assessment.
  • Commission FAQ explaining exemption validity, Annex III and IV roles, and application-specific use.
  • Commission FAQ explaining that exemptions are not granted for a company or whole EEE and that material limits are applied individually.
"Exemptions are granted for specific substances used in specific applications"
More quoted passages
"not for the whole EEE, nor for a company"
"maximum concentration values are applied to each of the homogeneous materials individually"
"Exemptions are now granted for a maximum validity period"
environment.ec.europa.eu6 citations
Referenced sections
  • Commission implementation source for exemption requests, renewal timing, reassessment factors, official exemption materials, and current process timing.
  • Commission implementation page for exemption procedure, reassessment factors, renewal timing, official exemption materials, and the lack of interim permission for a new exemption request.
  • Commission implementation source for the exemption procedure and official materials to check requested or renewed exemptions.
Show 3 more
  • Commission implementation page used to check official exemption and renewal materials instead of relying on an undated supplier statement.
  • Commission implementation source for exemption reassessment factors, application timing, and decision-duration guidance.
  • Commission source for time-limited exemption handling and reassessment process.
"Exemptions are limited in time"
More quoted passages
"Industry regularly applies for the renewal of exemptions"
"A decision on a RoHS exemption currently takes 18 to 24 months"
"Exemptions are limited in time and reassessed on a regular basis"
data.europa.eu3 citations
Referenced sections
  • Official source identifying EN IEC 63000:2018 as the harmonised standard for RoHS technical documentation.
  • Official source for EN IEC 63000 as the harmonised technical-documentation standard used for RoHS assessment.
  • Official source identifying EN IEC 63000:2018 for RoHS technical documentation.
"technical documentation required for assessing materials"
More quoted passages
"assessing materials, components and electrical and electronic equipment"
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