Sociedad Americana de Hirudoterapia

នាយកដ្ឋានឱសថ ចំណីអាហារ បរិក្ខារពេទ្យ និងគ្រឿងសម្អាង — ក្រសួងសុខាភិបាល

Cambodia DDF · Cambodia · asia pacific

Regulatory jurisdiction profileJurisdictional reference
Unregulatednational regulator

Cambodia's Department of Drugs, Food, Medical Devices and Cosmetics (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
Cambodia
Leech status
unregulated
Last ASH review
2026-05-27

Relevant Regulation Codes

  • Cambodian Law on the Management of Pharmaceuticals (2007, as amended)
  • Cambodian national medical device regulatory framework
  • ASEAN Medical Device Directive (AMDD) harmonised frameworks where applicable

Prescriber Requirements

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

Supply Chain & GMP

Cambodia DDF registration as applicable; Khmer and English-language labelling. Standard cold-chain conditions, with logistical constraints typical of tropical Mekong distribution.

Import/Export Rules

Cambodia DDF and General Directorate of Animal Health and Production clearance for live invertebrates; CITES Appendix II paperwork for Hirudo medicinalis / verbana.

Reimbursement Context

Cambodian Health Equity Fund and National Social Security Fund 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

Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.