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KBLI Navigator/Section C/32502
KBLI 32502★ Gold-Tier Intel

Medical, Dental, Orthopedic & Prosthetic Equipment Manufacturing

Industri Peralatan Kedokteran dan Kedokteran Gigi, serta Perlengkapan Ortopedi dan Prostetik

🏭 Section C — Manufacturing

In Bali: open to a PT PMA

✅Open· 100% ForeignLow RiskDirect Match🏝️✅Registrable in Bali· medium conf.

This code is for the manufacture of instruments and appliances used in medical, surgical, dental, and veterinary practices. It includes producing items like dental drills, eye testing equipment, syringes, sterilization and massage devices, and artificial respiration machines. It also covers the production of orthopaedic and prosthetic appliances, such as crutches, surgical belts, and permanent bone replacement plates.

Licensing & Requirements

What You Need

Risk LevelLow (Rendah)
License TypeNIB
ProcessingInstant
Foreign Ownership100% Open
AuthorityBKPM / OSS
PP28/2025 Licensing Data8 scales
Business scale:
MikroLow RiskNIB⏱ Otomatis
Post-License Obligations5
Memiliki bukti penyampaian wajib Data Industri tervalidasi setiap 6 (enam) bulan sekali sesuai peraturan perundang undangan di bidang perindustrian
Menjamin keamanan dan keselamatan alat, proses, hasil produksi, penyimpanan, serta pengangkutan, sesuai peraturan perundang undangan
Pencantuman spesifikasi, komposisi bahan dan/atau care label pada produk atau kemasan yang membuktikan dilaksanakannya pelayanan minimal pada pelanggan
Memiliki dokumen hasil kalibrasi peralatan quality control secara periodik atau hasil uji laboratorium independen atas produk yang dihasilkan secara periodik
Memiliki SOP keamanan dan keselamatan atas: a. Penyimpanan bahan baku berupa bahan kimia b. Penggunaan mesin/ peralatan c. Proses produksi
1
Company incorporation— PT PMDN / CV / Perorangan (local, WNI) — notary deed, AHU registration
2
NIB via OSS— register on oss.go.id, select this code, issued automatically (1–3 days)
3
NIB + Standard Certificate (Small, Medium-High risk)— Authority: Bupati/Walikota — 7 Hari
4
NIB + Standard Certificate (Medium, Medium-High risk)— Authority: Bupati/Walikota — 7 Hari
5
NIB + Standard Certificate (Large, Medium-High risk)— Authority: Gubernur — 7 Hari
6
Submit industrial data report every 6 months (Kemenperin)— post-license obligation
7
Menjamin keamanan dan keselamatan alat, proses, hasil produksi, penyimpanan, serta pengangkutan, ses...— post-license obligation
8
Memiliki dokumen hasil kalibrasi peralatan quality control secara periodik atau hasil uji laboratori...— post-license obligation

Authority by scale

PMA
2020 → 2025

Unchanged from KBLI 2020 — direct match.

Bali Intelligence

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Read Full Guide on Bali Zero↗

KBLI 2025 Manufacturing & Production: Industrial Business Codes

kita.balizero.com
Complementary Codes
Common Questions
Can foreigners operate a medical, dental, orthopedic & prosthetic equipment manufacturing business in Indonesia?
Yes. KBLI 32502 (Industri Peralatan Kedokteran dan Kedokteran Gigi, serta Perlengkapan Ortopedi dan Prostetik) is TERBUKA — open to 100% foreign ownership via PT PMA. No local Indonesian partner required.
What license is required for KBLI 32502?
KBLI 32502 has a Rendah risk classification. Required license: NIB. Processing time: Otomatis.
What is KBLI 32502?
KBLI 32502 is the Indonesian business classification code for "Industri Peralatan Kedokteran dan Kedokteran Gigi, serta Perlengkapan Ortopedi dan Prostetik" (Medical, Dental, Orthopedic & Prosthetic Equipment Manufacturing). It falls under Section C of KBLI 2025, the Indonesian Standard Industrial Classification updated by BPS (Regulation 7/2025). The June 2026 KBLI 2025 transition window has closed; operators should verify the code's current OSS/NIB treatment before relying on it for licensing, reporting, or amendments.
How did KBLI 32502 change from KBLI 2020 to 2025?
KBLI 32502 was mapped from previous code 32502 (KBLI 2020). This is a direct match — the code number and scope remained the same. The June 2026 KBLI 2025 transition window has closed. If an NIB still relies on legacy KBLI 2020 mappings, treat the migration as overdue and verify/remediate the OSS record before new license applications, amendments, LKPM, import approvals, or investor/worker sponsorship.

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🏢

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