licensing

SNI Certificate in Indonesia: Who Needs One, How to Get It

An SNI certificate in Indonesia is a condition of sale for some products. Check whether yours is one, who certifies it, and the steps from testing to the mark.

Jurisdiction
Indonesia
Last reviewed
10 Sept 2026
References
  • UU No. 20 Tahun 2014 tentang Standardisasi dan Penilaian Kesesuaian — the governing statute for standardisation and conformity assessment
  • PP No. 34 Tahun 2018 tentang Sistem Standardisasi dan Penilaian Kesesuaian Nasional — in force 20 July 2018. It expressly revokes PP No. 102 Tahun 2000, which is still cited in much of the guidance published on this subject

An SNI certificate in Indonesia confirms that a product meets the Standar Nasional Indonesia — the Indonesian national standard for its category. For some products it is a condition of selling here at all. For the rest it is optional, and worth having for reasons that are commercial rather than legal.

One thing is worth getting straight before anything else, because much of the guidance published on this subject gets it wrong. The standards agency does not issue your certificate. Three separate bodies have a hand in this and they are easy to confuse; which does what is set out below. The document you end up holding is formally an SPPT-SNI — the certificate entitling you to put the SNI mark on the product.

Does it apply to your product?

Mandatory and voluntary SNI compared
Mandatory SNIVoluntary SNI
What makes it apply A sectoral regulation applies a standard compulsorily to your product categoryThe standard exists and you choose to certify against it
Can you sell without it No. Goods in scope may not be legally distributed or sold uncertifiedYes
The SNI mark on the pack Required, and its use depends on holding the certificatePermitted once certified, and often asked for by retailers
Why companies do it Because the alternative is not sellingRetail acceptance, tender eligibility, and a quality claim that is independently checked

Whether a given product is in mandatory scope is not settled by a general list. It is set product by product, by the ministry responsible for that sector, applying a particular standard compulsorily. Electronics, children’s toys, construction materials, helmets and food packaging are the categories most often encountered — but the question that matters is whether your product’s own standard has been made compulsory, and that is checked against the applicable regulation for its classification rather than against a summary.

Who does what

Three different bodies appear in this process, and confusing them is the most common reason an application starts in the wrong place.

BSN develops and publishes the standards themselves. It is not a certifier and does not accredit anyone’s laboratory. KAN is the national accreditation committee: it assesses laboratories and certification bodies against international requirements and accredits them for defined scopes. An LSPro is a certification body so accredited, and it is the one that tests your case, audits your factory and issues the certificate.

Two consequences follow. A test report from a laboratory that is not accredited for your product’s scope will not support an application, however competent the laboratory. And an LSPro can only certify within the scope KAN has accredited it for, so the right first question is not “which LSPro is cheapest” but “which is accredited for this product”.

Who applies depends on where the product is made. A domestic manufacturer applies as itself — the Indonesian company that produces the goods. A foreign manufacturer or exporter is not shut out, but somebody has to be the applicant here, and where that means establishing an entity a foreign investment company is the usual vehicle. It needs to exist before it can apply for anything, which is a lead time in itself. The standards themselves are published by BSN.

How certification works

  1. You

    Identify the standard, and check the laboratory's scope

    Establish which SNI applies to the product and confirm the laboratory you intend to use is accredited for that scope. Getting this wrong invalidates everything built on it.

  2. Accredited laboratory

    Product testing

    The laboratory tests the product against the requirements of the applicable standard. What it tests depends on the product — chemical and mechanical safety for a toy, electrical safety and performance for an appliance.

  3. You, to the LSPro

    Application to the certification body

    You submit the application with your business identification number (NIB), issued through OSS — Online Single Submission, the government's licensing portal — along with the relevant manufacturing or import permits, product specifications and bill of materials, and quality management documentation. An ISO 9001 certificate is not compulsory but is routinely asked for.

  4. LSPro

    Factory audit

    The LSPro audits the production facility to confirm that quality control is consistent and that output can be traced. Where the factory is overseas, the audit goes there.

  5. LSPro

    Sampling, then issuance

    The LSPro takes samples from actual production and tests them against the standard. If everything holds it issues the certificate — which carries continuing surveillance obligations rather than being the end of the matter.

This cannot be done quickly, and that is the trap

Certification is not a form to be filed. It requires laboratory testing against the standard, and a factory audit that has to be scheduled with the certification body and travelled to if the plant is overseas. Neither compresses to suit a deadline. So for a product in mandatory scope — which may not be distributed or sold without it — the process belongs at the start of a launch or an import plan, not at the point where stock is already committed and waiting.

What it costs is the question we are asked most often and the one with no general answer, because the cost is assembled from the work actually required: the standard that applies and how much testing it calls for, the number of samples to be tested, whether the factory audit is domestic or has to travel, and whether the quality management documentation already exists or has to be built. A product tested against a short standard at a domestic factory and one tested against a long one at an overseas plant are not the same job.

⚠ The details on the application have to match what is registered against your business licence. OSS is the single record the rest is checked against, and an inconsistency there delays the application while it is reconciled. Keeping registered particulars current is ordinary corporate secretarial work, and it is cheaper than discovering a mismatch mid-application.

Where it goes wrong

The situation

What usually goes wrong

  • The laboratory was not accredited for the scope

    How to avoid itConfirm the laboratory's accreditation covers your specific product scope before any testing is commissioned, not after the report arrives. A report outside scope cannot be rescued and the testing is paid for twice.

  • Sector-specific requirements were missed

    How to avoid itThe applicable standard is only part of it: the ministry responsible for the sector may impose further conditions on the same product. Check the sectoral requirements alongside the standard rather than assuming the standard is the whole obligation.

  • The certificate was treated as a one-off

    How to avoid itCertification carries continuing surveillance obligations, and a lapse can put the certificate — and the right to use the mark — at risk. Put the surveillance dates and the renewal date in the same compliance calendar as your filing deadlines, on the day the certificate is issued.

What this means in practice

Almost none of the expense in this process comes from the requirement itself. It comes from doing the steps in the wrong order — commissioning testing before checking the laboratory’s scope, or discovering mid-application that what is registered against the business licence does not match what has been submitted. Both are checks that cost nothing at the point they are made and a great deal at the point they are missed.

The certificate is also not the finish. It carries surveillance obligations that run for as long as you rely on it, and the date those fall due belongs in the same calendar as every other filing deadline the business keeps.

Does your product need an SNI mark?

MAM sets up the company that holds the certificate and helps you plan the route, so you know what to expect before goods ship. A short call will tell you where to start.

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