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RoHS comparison table for 6 markets: EU, China, Korea, Japan, EAEU, California

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Customers ask: “My product has passed European RoHS, so if I sell it to China, Korea, Japan, Russia or California, do I need to do it again?” The honest answer is: depending on the market — because each place has its own “RoHS code”, which differs in the substance list, enforcement method and type of label required.

What makes this confusing is the general rules look similar: same few heavy metals, same 0.1% limit, same talk about “homogeneous material”. But just one detail difference – for example, where there are 6 substances limited, where there are 10 substances – the document proving conformity can no longer be used together.

This article builds a table comparing six markets at the principle level: EU, China, Korea, Japan, EAEU and California. The goal is not to replace the original document, but to let businesses know which documents they need to compare correctly before printing labels and signing declarations of conformity.

1. Six regulatory “roofs” — an overview first

The common point of all six places: they all limit a number of toxic substances in electrical and electronic products, and they all take common standards from four familiar heavy metals – lead, mercury, cadmium, hexavalent chromium. The difference lies in three questions:

  1. Limitations how much substance? And what substances?
  2. How to execute — prohibited from being placed on the market, mandatory labeling, nice conformity declaration?
  3. Who checks and any mark/label is the evidence?
Market Background text Number of substances restricted (principle) Main mechanism
EU Directive 2011/65/EU (RoHS 2, amended by (EU) 2015/863) 10 substances Ban on market + CE mark + technical documents
China GB 26572-2025 (mandatory, effective August 1, 2027), replaces GB/T 26572-2011 10 substances Mandatory limit + label according to SJ/T 11364
Korea Regulations on recycling of electrical and electronic equipment and vehicles (K-RoHS) 10 substances (gradually harmonized with the EU) Limit + conformity declaration
Japan J-Moss (marking system according to JIS C 0950) 6 substances Required label according to the specified product group
EAEU Technical regulations of the Eurasian Economic Union on substance restrictions in electrical and electronic products 6 substances Limit + EAC conformity mark
California (United States) Electronic Toxins Act (EWRA) 4 heavy metals Restricted to groups of devices with specified screens

Important note: The table above is the picture principle. The number of substances, product ranges and potency dates for each market change over time, so any specific details need to be met. Compare the current text verbatim before using it for a real batch.

2. First axis: substance list — 4, 6 or 10?

The most practical way of classifying is to count from the “core” out:

  • Heavy metal 4 core: lead (Pb), mercury (Hg), cadmium (Cd), hexavalent chromium (Cr(VI)). Almost every market limits these four substances.
  • Up to 6 substances: Add two groups of brominated flame retardants: PBB and PBDE. This is the popularity of “6 elements” type programs — common in Japan (J-Moss) and EAEU.
  • Up to 10 substances: add four phthalates (DEHP, BBP, DBP, DIBP). This is the EU level after 2015, and is also the direction that China and South Korea have followed.

The practical consequences are clear: one product REACHing 6 substances is not necessarily achieving 10 substances — because there are four phthalates left. On the contrary, products with 10 substances usually cover the requirement of 6 substances (because 6 substances are a subset of 10), unless That market has its own qualities beyond the EU list. Therefore, the strongest set of documents to go to many markets is the set that proves all 10 substances, plus separate comparisons for each place.

Material sample trays on the inspection table: metal parts, plastic pieces, cables and small circuit boards
From a core of 4 heavy metals to 6 substances and then 10 substances – each additional level is a new group of substances that must be proven.

3. Second axis: limit and calculation — almost identical

Here’s the good news: most markets use the same limits and the same calculation logic.

Factor Popularity level
General limit 0.1% by mass (equivalent to 1,000 ppm)
Particularly cadmium 0.01 % (equivalent to 100 ppm) — 10 times tighter
How to calculate Theo homogeneous material, not the whole product

Because of the same limit and the same calculation method, Test results and test methods are reproducible between markets. What has to be redone is only part conformity conclusion: compare the results with the correct substance list and the correct exemption list of that market.

4. Third axis: enforcement mechanism — ban, label or declare?

This is where markets differ the most, and is also where businesses often misunderstand.

Mechanism What does it mean? Typical market
Prohibited from being placed on the market Exceeding the limit without an exemption cannot be sold; Must demonstrate compliance EU
Mandatory limit with label Must meet the limit and print the board/label according to regulations China
Declaration of conformity Enterprises self-assess and declare and are responsible for the information Korea
Labeling required The focus is information disclosure substance content for buyers to know Japan (J-Moss)

Points to remember: “labeled” is not the same as “allowed to exceed the limit”. In some systems, the labeling is to declare the substance status, not the license. Confusion between “must be labeled” and “exempt” is a common reason why goods are detained at the border.

Desk with three types of blank documents: manifest, declaration sheet and an unprinted label
Three mechanisms, three types of documents: prohibition of technical documents, declaration of conformity, and labeling to disclose substance information.

5. Fourth axis: labels and conformity marks

Market Typical markings/labels Note the principle
EU CE mark CE covers RoHS; accompanied by declaration of conformity and technical documents
China Label according to SJ/T 11364 (label style EFUP/substance table) The label is covered by national mandatory regulations
Korea Label/mark of the K-RoHS compliance declaration system Associated with the declaration obligations of the manufacturer/importer
Japan J-Moss mark (blue/orange according to substance state) The mark shows whether the product is in excess or not
EAEU EAC mark A common mark for the entire block
California There is no separate CE mark of conformity Enforcement through regulatory agency requirements and procurement conditions

A note about label language: absolutely do not label yourself “certified” or “certified” if there is actually only a test report. Each market has its own regulatory wording, and misstatements can be considered misleading.

6. Detailed comparison table of six markets

Criteria EU China Korea Japan EAEU California
Number of substances (principle) 10 10 10 6 6 4
Specific cadmium 0.01 % Yes Yes Yes Yes Yes Yes
How to calculate Homogeneous materials Homogeneous materials Homogeneous materials Homogeneous materials Homogeneous materials Homogeneous materials
Mechanism Ban + CE Required + label Limit + declaration Label Limit + EAC Restrictions by device group
Scope Open scope for EEE Product grouping According to EEE category Designated product group By product category Devices with screens (regulated group)
Primary evidence Technical documents + declaration of conformity Test report + label Declaration of conformity + report Label + internal data Profile + EAC marking Documents according to agency requirements

How to read the table: the first four lines are almost identical, the “mechanism” and “scope” lines are where the difference is. In other words, Test results can be used everywhere, but the proof and type of labels must be made according to each place.

7. Why do some markets only stop at 6 substances?

Japan (J-Moss) and EAEU keep the level of 6 substances while the EU has increased to 10. There are two common reasons:

  • Management philosophy: Some places choose to “announce so the market can self-regulate” (label) instead of completely banning it. J-Moss is a prime example — the focus is on substance information transparency.
  • Update cadence: Trade blocs update substance lists according to their own schedules. When the EU added phthalates in 2015, other markets took more time to harmonize.

So don’t assume “the moves that follow will always keep 6 suits”. China is the latest example of how a market can go from six to 10 substances and make it mandatory — so the safe strategy is Designed according to 10 substances and track changes in each location.

8. 5-step process when selling to many markets

  1. List target markets for each product code, with sales channel (direct, import, e-commerce platform).
  2. Determine the highest “quality level”. must meet (4, 6 or 10) and take that as the design goal.
  3. Establish a common material data set at the homogeneous material level, enough to answer for all 10 group substances.
  4. Compare individual exemptions for each market — exemptions are not shared.
  5. Prepare labels and separate statements For each market, clearly state the compared legal basis.
Export warehouse with plain cartons on pallets and forklifts in the background, no text or logo
One common set of material data, multiple sets of individual labels and claims — how to go to multiple markets without having to start over.

9. Five common misconceptions

  1. “If you meet EU RoHS, you can sell everywhere.” Not really — the 10-substance market is convenient, but places that require private labels (China, Japan) still have to comply with the label part.
  2. “6 substances are enough for everyone because that is the international standard.” Wrong — EU, China, Korea are already at level 10 substances.
  3. “Mandatory labeling means being allowed to exceed the limit.” False — the label is a disclosure, not a license.
  4. “Shared exemption across markets.” False — each has its own exemption category and its own update schedule.
  5. “The number of substances and potency markers remain unchanged.” Incorrect — these are frequently edited documents; Must check each batch.

10. Frequently asked questions

If we have reached 10 substances according to the EU, do we have to retest for China?

There is usually no need for technical retesting, because the substance list is similar and the methods are shared. But the limit, product range and label requirements must be reconciled according to current Chinese regulations.

Is J-Moss a mandatory substance limiter like RoHS?

Not in the same way. J-Moss is the system label by designated product group: the focus is on disclosing information on substance content, different from the EU-style market ban mechanism.

How is California different from other US states?

California has its own laws on toxics in electronic devices, focusing on the regulated group of devices with screens, rather than a federal RoHS set. The scope and list of equipment need to be compared with current state documents.

Does this table replace reading the original text?

No. This is a framework for orientation. All substance numbers, validity dates and label requirements must be compared verbatim to the current effective text in each market before application.

At what level should the product be designed?

As high as the target market requires — typically 10 substances — and keep the material data set at a consistent material level. This method helps reuse data when opening new markets.

11. Conclusion

Six markets, six sets of regulations, but same technical core: four heavy metals, limit 0.1 % (Cd 0.01 %), calculated on homogeneous material. The difference focuses on number of substances (4, 6 or 10), enforcement mechanism (ban, label, declare) and label type.

Pragmatic strategy: design and collect data for 10 substances at a uniform material level, then separate labels and claims for each market. So businesses only have to do the technical part once, instead of trying again for each location.

And the principle cannot be abandoned: all legal details must be compared verbatim to the current document. The reference table helps you know what to read — it doesn’t read it for you.

References

  • Directive 2011/65/EU (RoHS 2) and Directive (EU) 2015/863 — EU
  • GB 26572-2025 and label set SJ/T 11364 — China
  • Regulations on recycling of electrical, electronic and vehicle equipment (K-RoHS) — Korea
  • J-Moss (JIS C 0950) — Japan
  • Technical regulations of the Eurasian Economic Union on substance restrictions in electrical and electronic products (EAC mark)
  • Electronic Toxins Act (EWRA) — California, United States

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    Disclaimer

    This article is an interpretive content compiled by us; not legal advice. The number of substances, limits, scope and validity milestones for each market are stated at the principle level and It is necessary to compare the current text verbatim before applying to specific products.

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