American Society of Hirudotherapy

Badan Pengawas Obat dan Makanan — National Agency of Drug and Food Control

BPOM · Indonesia · asia pacific

Regulatory jurisdiction profileJurisdictional reference
Traditional medicinenational regulator

Indonesia's national agency for drug and food control — leech-specific regulatory pathway has not been independently verified by ASH; pengobatan tradisional has a separate framework under the Ministry of Health.

Regulatory Profile

Agency type
national regulator
Region
asia pacific
Country
Indonesia
Leech status
traditional medicine
Last ASH review
2026-05-25

Relevant Regulation Codes

  • Undang-Undang Kesehatan (Indonesian Health Law)
  • Indonesian Ministry of Health regulations on traditional medicine (pengobatan tradisional)

Prescriber Requirements

  • Indonesian Medical Council (KKI)-registered physician for biomedical use
  • Traditional medicine practitioners (battra / hattra) registered under the Ministry of Health may have separate scope; specific hirudotherapy authorisation not independently verified by ASH

Supply Chain & GMP

BPOM registration if classified as a medical device; Bahasa Indonesia labelling.

Import/Export Rules

BPOM import licence plus Quarantine Authority for live invertebrates; CITES Appendix II paperwork.

Reimbursement Context

BPJS Kesehatan (national health insurance) coverage for hirudotherapy not independently verified by ASH.

ASH Editorial Notes

Indonesia recognises three categories of traditional medicine practitioners (battra empiris, battra ramuan, battra ketrampilan) under Ministry of Health regulations. Whether leech therapy is regulated as a traditional medicine modality or as a medical device under BPOM has not been independently verified by ASH.

Related Jurisdictions

This website provides educational information and does not constitute medical advice, diagnosis, or treatment recommendations. Medicinal leech therapy carries clinically meaningful risks and should be performed only by qualified clinicians under institutionally approved protocols. FDA 510(k) clearance for medicinal leeches is limited to specific indications; investigational and off-label discussions are labeled accordingly. For patient-specific guidance, consult a qualified healthcare provider.