Американское общество гирудотерапии

ກົມອາຫານ ແລະ ຢາ — ກະຊວງສາທາລະນະສຸກ

Laos FDD · Laos · asia pacific

Regulatory jurisdiction profileJurisdictional reference
Unregulatednational regulator

Laos' Food and Drug Department (Ministry of Health) — leech-specific regulatory pathway has not been independently verified by ASH; medicinal leeches fall under the general national pharmaceutical and medical device framework as appropriate.

Regulatory Profile

Agency type
national regulator
Region
asia pacific
Country
Laos
Leech status
unregulated
Last ASH review
2026-05-27

Relevant Regulation Codes

  • Lao PDR Law on Drugs and Medical Products (Law No. 38/NA, 2011, as amended)
  • Lao PDR national medical device regulatory framework
  • ASEAN Medical Device Directive (AMDD) harmonised frameworks where applicable

Prescriber Requirements

  • Lao Medical Council–registered physician — order required for any biomedical device application
  • Allied health professional application under physician supervision per institutional protocol

Supply Chain & GMP

Laos FDD registration as applicable; Lao and English-language labelling. Standard cold-chain conditions, with logistical constraints typical of tropical Mekong distribution.

Import/Export Rules

Laos FDD and Department of Livestock and Fisheries clearance for live invertebrates; CITES Appendix II paperwork for Hirudo medicinalis / verbana.

Reimbursement Context

Lao National Health Insurance (NHI) coverage depends on inpatient bundling; outpatient hirudotherapy is generally not separately reimbursed.

ASH Editorial Notes

Leech-specific pathway not independently verified by ASH; falls under general medical device / traditional medicine framework as appropriate. South-East Asian regulatory frameworks are progressively coordinating through the ASEAN Medical Device Directive (AMDD); whether this captures live-organism medical devices has not been independently mapped by ASH.

Related Jurisdictions

Этот сайт предоставляет образовательную информацию и не является медицинской консультацией, диагнозом или рекомендацией по лечению. Гирудотерапия сопряжена с клинически значимыми рисками и должна проводиться только квалифицированными клиницистами в рамках институционально утверждённых протоколов. Разрешение FDA 510(k) для медицинских пиявок ограничено определёнными показаниями; обсуждения исследовательского и нелицензионного применения отмечены соответствующим образом. Для индивидуальных медицинских рекомендаций обратитесь к квалифицированному медицинскому специалисту.