KBLI 2020 · 5-digit class

32502Medical and Dental Equipment, Orthopaedic, and Prosthetic Supplies Industry

Industri Peralatan Kedokteran Dan Kedokteran Gigi, Perlengkapan Orthopaedic Dan Prosthetic

Last updated · Sourced from OSS Indonesia

$4b

For foreign investors · KBLI 32502
100% PMA

Yes — open to PMA up to 100%.

Operating license routes through Ministry of Industry, not OSS — Emerhub handles the application end-to-end.

Foreign ownership
100% PMA
Sector regulator
Ministry of Industry (Kemenperin)
Min. paid-up capital
IDR 2.5B paid-up · BKPM Reg. 5/2025
Issuing authority for PMA
Minister/Head of Agency
Ministry-issued
Risk + license type
Medium-High·NIB + Verified Standard Cert.
Setup timeline
PT PMA 4–8 weeks; Emerhub files the verified Standard Certificate (1–2 months ministry review).

What's specific to this sector

  • 01

    Industry data reporting via SIINas every 6 months.

  • 02

    BPOM registration required for any food, drug, cosmetic, or medical device produced.

  • 03

    Halal certification mandatory for most consumable products.

Get a verified setup plan for KBLI 32502Read the full regulatory profile

KBLI 32502 at a glance

KBLI code
32502
Taxonomy version
KBLI 2020
Activity (English)
Medical and Dental Equipment, Orthopaedic, and Prosthetic Supplies Industry
Activity (Indonesian)
Industri Peralatan Kedokteran Dan Kedokteran Gigi, Perlengkapan Orthopaedic Dan Prosthetic
Category
Manufacturing Industry
Risk level (Large scale, PMA)
Medium-High
Foreign ownership status
Fully open to PMA (100%)
Minimum capital (PT PMA)
IDR 2.5 billion paid-up + IDR 10 billion+ commitment per KBLI (BKPM Reg. 5/2025)
Primary licensing instrument
NIB
Issuing authority (PMA)
Minister/Head of Agency
Tax incentive eligibility
None recorded
Last verified
April 24, 2026
Source: OSS Indonesia + BPS Peraturan 7/2025 + BKPM
§ 01

Foreign investment rules

Indonesia's BUPM (Investment Business Fields) regulation places this code into one of five tracks. The track determines whether a foreign investor (PMA) can operate in this activity at all, and under what conditions.

Status · open

Fully open to foreign investment

KBLI 32502 is not on Indonesia's closed, conditional, SME-reserved or partnership-required schedules. A foreign investor may incorporate a PT PMA with up to 100% foreign ownership and operate in this activity directly.

This KBLI is not listed in any restricted, closed, SME-reserved or partnership-required schedule under Pres. Reg. 10/2021 (as amended). A 100% foreign-owned PT PMA may operate in this activity, subject to the licensing requirements shown below. BKPM's default minimum capital is IDR 2.5 billion paid-up with IDR 10 billion+ total investment commitment per KBLI realised over time, but sector regulators (OJK, ESDM, BPOM, Kominfo, etc.) can set higher minimums for specific activities — we confirm the actual figure before incorporation.
§ 02

How we handle your KBLI 32502 setup

Emerhub is a corporate-services provider in Indonesia. We do the legal and regulatory legwork for foreign investors so you can focus on the business itself. Here's what the engagement looks like.

  1. 1

    Confirm the optimal structure for your business

    2–3 business days

    We confirm KBLI 32502 is the right primary code for your business, advise on secondary codes you may also need, and finalize the holding structure with you before any filing.

    What we need from you
    • Founders' passport copies and proof of residence
    • Intended share split and board composition
  2. 2

    Incorporate your PT PMA

    7–10 business days

    We draft the Articles of Association before a notary, register the entity with the Ministry of Law & Human Rights (Kemenkumham), and obtain the company's tax ID (NPWP). Under BKPM Reg. 5/2025, paid-up capital is IDR 2.5 billion (~USD 160K) — the cash actually deposited at incorporation. The IDR 10 billion+ figure many sources still cite is the total investment commitment per KBLI, realised over time via your LKPM reports.

    What we need from you
    • Powers of attorney (we prepare; you sign and notarize)
    • Director / commissioner appointment letters
    • Initial capital deposit confirmation
  3. 3

    We obtain your NIB

    1–2 business days

    We file the OSS application with KBLI 32502 as your primary business activity, complete the risk-based assessment, and collect the NIB (Business Identification Number) for you — typically within hours of submission. You don't need to touch the OSS portal.

    What we need from you
    • Office address (virtual office acceptable for many KBLIs; we can arrange one)
  4. 4

    Secure your Standard Certificate (Verified)

    7+ business days

    NIB is issued for the preparation stage. To begin commercial operations, the operator must obtain a Sertifikat Standar that has been verified by the competent ministry. The verification step typically requires a site or document inspection. Operating with NIB alone is not legally compliant. We prepare the application bundle, liaise with the competent ministry, and chase issuance through to the certificate. Statutory turnaround: 7 business days — real-world timing typically runs longer when site inspections or additional clarifications are requested.

    What we need from you
    • Technical documentation specific to your operation
    • Appointment of a Penanggung Jawab Teknis (PJT — technical responsible person)
  5. 5

    Hand-off to ongoing compliance

    Ongoing

    Post-launch we run your monthly tax filings, quarterly LKPM (Investment Activity Reports), annual general meeting (RUPS), and any sector-specific reporting. You get a single point of contact and a monthly compliance digest — no Indonesian-language paperwork on your desk.

Get an exact quote and timeline for KBLI 32502, scoped to your specific business plan.
Request a quote
§ 03

What is KBLI 32502?

A plain-English explanation of this classification and the businesses it covers.

KBLI 32502 (Industri Peralatan Kedokteran Dan Kedokteran Gigi, Perlengkapan Orthopaedic Dan Prosthetic) is the 5-digit Indonesian Standard Industrial Classification code for medical and dental equipment, orthopaedic, and prosthetic supplies industry. It sits within Manufacturing Industry under the subgroup Medical and Dental Instruments and Supplies Industry. (major group 32) in the official KBLI 2020 taxonomy maintained by Statistics Indonesia (BPS).

$4b

Who needs KBLI 32502?

Any Indonesian or foreign-owned entity that intends to operate in medical and dental equipment, orthopaedic, and prosthetic supplies industry as a primary or secondary business activity must select this code on its NIB (Business Identification Number). The selected code determines the licensing instruments required, the issuing authority, and the ongoing compliance obligations.

Why does the code matter?

Indonesia's OSS Risk-Based Approach uses the KBLI code to determine three things: (1) whether foreign investment is permitted and at what cap, (2) the risk-based licensing instruments required, and (3) the authority that issues each instrument. Choosing the wrong code can delay or invalidate your license.

§ 04

Under the upcoming KBLI 2025

Indonesia's BPS published the new KBLI 2025 taxonomy in early 2025. OSS, BKPM and the operating ministries have not yet adopted it — KBLI 2020 remains the active standard for business registration. This is what's coming for this specific code.

Carried forward into KBLI 2025

KBLI 32502 retains the same code number and scope in the new taxonomy. The activity description, hierarchy, and intended use of the code are preserved.

  • ·Continue using 32502 for current registrations under KBLI 2020.
  • ·When OSS adopts KBLI 2025 (timing not yet announced), no migration is required for this code.
  • ·Risk level, permits, and authority routing shown above remain in effect under both taxonomies.

When OSS adopts KBLI 2025, we'll migrate your existing entity to the appropriate successor code as part of ongoing compliance — no action needed on your end now.

Talk to a specialist
§ 02

Risk level by business scale

Indonesia's OSS Risk-Based Approach assigns a separate risk level for each of the four business scales. The licensing instruments required (NIB, Standard Certificate, Operating License) are determined by the risk level. Foreign-owned entities (PT PMA) must register at the Large scale, so the rightmost column applies to most foreign investors.

01

Micro

Usaha Mikro
≤ IDR 2 B turnover
Medium-High risk
NIB + ministry-verified Standard Certificate before invoicing.
02

Small

Usaha Kecil
IDR 2 – 15 B
Medium-High risk
NIB + ministry-verified Standard Certificate before invoicing.
03

Medium

Usaha Menengah
IDR 15 – 50 B
Medium-High risk
NIB + ministry-verified Standard Certificate before invoicing.
04

Large

PMA scale
Usaha Besar
IDR > 50 B
Medium-High risk
NIB + ministry-verified Standard Certificate before invoicing.
What does each risk level require to operate? ›
Low. NIB alone is sufficient for both preparation and commercial operation. Issued instantly via OSS.
Medium-Low. NIB enables preparation only. Commercial operation requires a self-declared Sertifikat Standar (Standard Certificate). Operating with NIB alone is not legally compliant.
Medium-High. NIB enables preparation only. Commercial operation requires a Sertifikat Standar verified by the competent ministry — typically with a site or document inspection.
High. NIB enables preparation only. Commercial operation requires a full Operating License (Izin) issued by the competent ministry after substantive review.
Beyond OSS, sector-specific permits commonly apply on top — e.g. SBU for construction, BPOM for food/cosmetics/medicines, OJK for financial services, IUP for mining, PSE for digital services. See the industry-specific guidance below for what applies to this KBLI.
§ 05

Licensing requirements in detail

Specific permits, application requirements and ongoing obligations vary by business scale and the sub-activity within this KBLI. We file these on your behalf — this section is for transparency on what we'll be handling. Switch between scales below; by default we show Large (the PMA scale).

What's required to operate
NIB
Preparation only — additional permit needed below
Standard Certificate (Verified)
Important: NIB is issued for the preparation stage. To begin commercial operations, the operator must obtain a Sertifikat Standar that has been verified by the competent ministry. The verification step typically requires a site or document inspection. Operating with NIB alone is not legally compliant.
Processing time
7Days
Statutory turnaround

Application requirements

8

Documents and capabilities you must demonstrate at registration

  • 01Have a document outlining the plan for the type, specifications, quantity, and source of raw materials, as well as the source and amount/volume of energy and water needed to carry out industrial business activities for 1 (one) production cycle or for a duration of 6 (six) months ahead.
  • 02Have documents in the form of: a) machine specifications and/or equipment list b) photos of machines/equipment and c) sales/rental agreements that prove: 1) control (ownership/rental) of machines to produce health equipment industry products and quality testing equipment 2) conformity of installed production capacity with business data
  • 03Have an organizational structure document for Human Resources that minimally consists of: a) Company leadership, person in charge of production, person in charge of quality control, person in charge of Human Resources development and/or b) Person in charge of marketing.
  • 04Have a flowchart document: a) Procurement, receipt, storage of raw materials b) Production process c) Quality control process d) Packaging, storage, transportation, and distribution of production results
  • 05Possess documentation in the form of photos proving the availability of occupational accident handling facilities and rest areas for workers.
  • 06Have documents outlining the specifications and intended use of the produced goods.
  • 07Have a work agreement document that proves the ownership of employees working as Technical Responsible Person (PJT) for Medical Devices.
  • 08Have a Statement of Commitment to Comply with Good Manufacturing Practices (GMP) for Medical Devices.

Ongoing obligations

6

Compliance and reporting duties throughout operation

  • 01Have proof of submission of mandatory validated Industrial Data every 6 (six) months in accordance with the laws and regulations in the industrial sector.
  • 02Ensure the safety and security of equipment, processes, production results, storage, and transportation, in accordance with applicable laws and regulations.
  • 03Possess periodic calibration documents for quality control equipment or periodic results from independent laboratory tests on the produced products.
  • 04Have a document in the form of a disaster evacuation SOP, including the arrangement of workplace safety signs.
  • 05Having a Health Equipment Quality Management System certificate (ISO 13485)
  • 06Have at least 1 (one) Technical Responsible Person who has a Good Manufacturing Practice (GMP) training certificate for Medical Devices.

Issuing authority

The authority that issues the license depends on your situation.

AuthorityApplies when
Minister/Head of AgencyThe industrial location is situated within a cross-border area between provinces.
Minister/Head of AgencyForeign Investment
GovernorThe industrial location is in the relevant province.
§ 05

Auxiliary permits (PB UMKU)

PB UMKU permits sit on top of the main NIB and Sertifikat Standar — each is issued by a different ministry, and only when a specific operational activity is performed. This KBLI carries 5 candidate permits across 1 regulator; most operations only need a handful. Emerhub maps your operation to the exact set, files them, and tracks renewals.

Health & Medical Devices

5 permits

Ministry of Health (Kemenkes / BPOM). Applies to manufacturing, importing, distributing, or operating medical devices, hospitals, clinics, diagnostic services, and pharmacies. Most device permits are class-based (Class A/B/C/D); facility permits attach to the specific site.

§ 08

Common questions about KBLI 32502

What is KBLI 32502?

KBLI 32502 (Industri Peralatan Kedokteran Dan Kedokteran Gigi, Perlengkapan Orthopaedic Dan Prosthetic) is the 5-digit Indonesian Standard Industrial Classification code for medical and dental equipment, orthopaedic, and prosthetic supplies industry. It sits within the Manufacturing Industry category in the official KBLI 2020 taxonomy maintained by Badan Pusat Statistik (BPS).

Can foreign investors operate under KBLI 32502?

Yes — KBLI 32502 is fully open to foreign investment. A PT PMA may operate with up to 100% foreign ownership, subject to BKPM Reg. 5/2025 capital requirements (IDR 2.5 billion paid-up + IDR 10 billion+ commitment per KBLI).

What is the risk level of KBLI 32502?

KBLI 32502's risk levels per business scale: Micro Medium-High, Small Medium-High, Medium Medium-High, Large Medium-High. Foreign-owned entities (PT PMA) must register at the Large scale.

What licenses does KBLI 32502 require?

NIB only — KBLI 32502 is a low-risk activity in OSS RBA, so the Business Identification Number alone suffices for operational licensing.

What is the minimum capital for a PT PMA under KBLI 32502?

BKPM Reg. 5/2025 default applies: IDR 2.5 billion paid-up capital at incorporation + IDR 10 billion+ total investment commitment per KBLI registered, realized over time and reported quarterly via LKPM.

How long does it take to register a business under KBLI 32502?

PT PMA setup typically takes 4-8 weeks: AHU registration (1-2 weeks), NIB issuance via OSS (immediate to 1 week), bank account opening (2-4 weeks). The licensing cycle for KBLI 32502 specifically takes 7 days at the Large business scale.

Is KBLI 32502 eligible for Indonesian tax incentives?

Not on the Tax Holiday or Tax Allowance priority lists. KBLI 32502 businesses pay the standard 22% PPh Badan; Super Tax Deduction (300% R&D / 200% vocational training) may still apply for qualifying expenses.

Which authority issues the KBLI 32502 license?

Authority depends on the investor profile. For PMA: Minister/Head of Agency. For domestic SME scale: typically Governor (for Provincial scope) or Regent/Mayor (Regency/City scope). Specific mapping is in §1 of this page.

What other permits beyond the NIB does KBLI 32502 need?

Beyond the NIB, KBLI 32502 carries 5 PB UMKU permits across 1 sector regulator: Health & Medical Devices (5). Most operations only need 2-4 of these — the relevant set depends on which specific activities you actually perform; Emerhub maps the right subset before filing.

What KBLI codes are similar to 32502?

KBLIs in the same subgroup 3250: 32501 (Furniture Industry for Medical and Dental Operations and Care); 32503 (Eyewear Industry); 32509 (Medical and Dental Equipment Industry and Other Supplies). These are closely related activities — see the related-codes section below for full list.

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Get your KBLI 32502 setup handled end-to-end.

Emerhub is a corporate-services provider in Indonesia. We handle PT PMA incorporation, licensing, tax registration and monthly compliance — so you focus on operating the business.
Get a quote for KBLI 32502