Sociedad Americana de Hirudoterapia

Health Sciences Authority

HSA · Singapore · asia pacific

Regulatory jurisdiction profileJurisdictional reference
Medical device clearednational regulator

Singapore's health sciences regulator — leech therapy supervised under the Health Products Act 2007 with separate licensing for TCM practitioners using leeches in clinical practice.

Regulatory Profile

Agency type
national regulator
Region
asia pacific
Country
Singapore
Leech status
medical device cleared
Last ASH review
2026-05-25

Relevant Regulation Codes

  • Health Products Act 2007 (Cap. 122D)
  • Health Products (Medical Devices) Regulations 2010
  • Traditional Chinese Medicine Practitioners Act 2000

Prescriber Requirements

  • Singapore Medical Council–registered MD or TCM Practitioners Board–registered TCM Practitioner
  • Allied health applies under physician order in hospitals (e.g., Singapore General Hospital plastic-surgery service)
  • TCM scope explicitly includes leech therapy under TCM Board guidance

Supply Chain & GMP

Class B / Class C medical-device registration under HSA — depending on intended use. GDPMDS-compliant distributor. English-language labelling.

Import/Export Rules

HSA Import Licence + Agri-Food and Veterinary Authority (AVA, now Singapore Food Agency) clearance for live invertebrates. CITES Appendix II permits.

Reimbursement Context

MediShield Life and MediSave cover inpatient procedures under standard DRG. TCM-delivered leech therapy is private-pay; some Medisave-approved chronic-disease management programmes touch peripherally.

ASH Editorial Notes

Singapore's parallel-track regulation (HSA for biomedical, TCM Board for traditional medicine) is among the world's most coherent dual-stream frameworks; leech therapy operates in both lanes.

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.