American Society of Hirudotherapy

Agência Nacional de Vigilância Sanitária

ANVISA · Brazil · latin america

Regulatory jurisdiction profileJurisdictional reference
Medical device clearednational regulator

Brazil's national health-surveillance agency — leech therapy regulated as a medical device with parallel coverage under the SUS Practices Integrativas e Complementares (PICS) policy.

Regulatory Profile

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

Relevant Regulation Codes

  • Lei nº 9.782/1999 — cria a ANVISA
  • Lei nº 6.360/1976 — vigilância sanitária a que ficam sujeitos os medicamentos
  • RDC nº 751/2022 — classificação de risco e regularização de dispositivos médicos
  • Política Nacional de Práticas Integrativas e Complementares no SUS — PNPIC (Portaria 971/2006)

Prescriber Requirements

  • CRM-registered médico prescription required
  • Enfermeiro/a (RN) application under physician's order; complementary-practice diplomas accredited via Ministério da Saúde / SUS
  • Hirudoterapia explicitly listed among PICS modalities under Portaria 971/2006

Supply Chain & GMP

ANVISA device registration (Cadastro / Registro) per RDC 751/2022; AFE (Autorização de Funcionamento da Empresa) for distributors. Portuguese-language labelling mandatory.

Import/Export Rules

Import via VICOMEX system + Ministério da Agricultura, Pecuária e Abastecimento (MAPA) clearance for live invertebrates. CITES via IBAMA.

Reimbursement Context

SUS (Sistema Único de Saúde) covers hirudoterapia in some municipalities under PNPIC implementation — São Paulo, Rio de Janeiro, and several Northeast capitals have funded programmes. Private insurance (saúde suplementar) variable.

ASH Editorial Notes

Brazil is Latin America's leading hirudotherapy jurisdiction — PNPIC policy puts the country in a small group (with Switzerland and Russia) that explicitly funds leech therapy as a complementary public-health service.

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.