American Society of Hirudotherapy

Dirección General de Medicamentos, Insumos y Drogas

DIGEMID · Peru · latin america

Regulatory jurisdiction profileJurisdictional reference
Medical device clearednational regulator

Peru's medicines, supplies and drugs directorate — leech therapy supervised under Ley General de Salud and complementary-medicine framework, with DIRESA-level enforcement.

Regulatory Profile

Agency type
national regulator
Region
latin america
Country
Peru
Leech status
medical device cleared
Last ASH review
2026-05-25

Relevant Regulation Codes

  • Ley General de Salud, Ley Nº 26842
  • Ley Nº 29459 — Productos Farmacéuticos, Dispositivos Médicos y Productos Sanitarios
  • DS 016-2011-SA — reglamento para el registro de dispositivos médicos

Prescriber Requirements

  • Colegio Médico del Perú-registered MD prescription required
  • Enfermero/a application under physician's order
  • Medicina complementaria framework administered via EsSalud's CAMEC programme

Supply Chain & GMP

Registro Sanitario via DIGEMID; importer requires Autorización Sanitaria. Spanish-language labelling.

Import/Export Rules

VUCE customs portal + SENASA agricultural-health clearance for live invertebrates. CITES via SERFOR (Servicio Nacional Forestal y de Fauna Silvestre).

Reimbursement Context

EsSalud's CAMEC (Centro de Atención de Medicina Complementaria) network has historically delivered hirudoterapia in regional hospitals — Peru is unusual in Latin America for having an in-system complementary-medicine clinical service.

ASH Editorial Notes

EsSalud's CAMEC programme is a rare institutional home for hirudotherapy in the Latin American public sector; ASH research collaboration with Universidad Peruana Cayetano Heredia under discussion (Q2 2026).

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.