American Society of Hirudotherapy

Ministry of Food and Drug Safety

MFDS · South Korea · asia pacific

Regulatory jurisdiction profileJurisdictional reference
Traditional medicinenational regulator

South Korea's drug-safety regulator (formerly KFDA) — leech therapy practised within the Korean Medicine (한의학 / Hanui) tradition; Hirudo medicinalis listed in the Korean Pharmacopoeia.

Regulatory Profile

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

Relevant Regulation Codes

  • Pharmaceutical Affairs Act (약사법)
  • Medical Service Act (의료법) — defines parallel MD / KMD scope
  • Korean Pharmacopoeia, 11th ed., monograph 거머리 (geo-meo-ri)

Prescriber Requirements

  • Korean Medicine Doctor (KMD / 한의사) is the principal prescriber within Hanui system
  • Biomedical physician (MD / 의사) can also prescribe; dual licensing rare
  • Allied health (nurses) under physician's order in hospital settings

Supply Chain & GMP

KMD pharmacies (한약방) traditionally stock dried leech preparations; live-leech supply chain is limited to specialised tertiary hospitals (Seoul National University Hospital, Asan Medical Centre).

Import/Export Rules

Imports require MFDS permission and Animal and Plant Quarantine Agency (APQA) clearance. CITES paperwork for Hirudo spp.

Reimbursement Context

National Health Insurance Service (NHIS / 국민건강보험공단) covers Hanui treatments selectively — hirudotherapy reimbursement depends on diagnostic code and provider type; reconstructive-surgery indications generally covered when delivered by MD.

ASH Editorial Notes

MFDS was renamed from KFDA in 2013; both terms appear in older literature. Korea operates parallel biomedical (MD) and Korean Medicine (KMD) systems — both have leech-therapy scope.

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.