Sociedad Americana de Hirudoterapia

Instituto Nacional de Higiene Rafael Rangel — Venezuela

INHRR · Venezuela · latin america

Regulatory jurisdiction profileJurisdictional reference
Unregulatednational regulator

Venezuela's Instituto Nacional de Higiene Rafael Rangel (Ministerio del Poder Popular para la Salud) — 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
latin america
Country
Venezuela
Leech status
unregulated
Last ASH review
2026-05-27

Relevant Regulation Codes

  • Venezuelan Ley de Medicamentos (Decreto N° 1.469)
  • Venezuelan Reglamento de la Ley de Medicamentos
  • Venezuelan national medical device regulatory framework

Prescriber Requirements

  • Venezuelan Colegio de Médicos–registered physician — order required for any biomedical device application
  • Allied health professional application under physician supervision per institutional protocol

Supply Chain & GMP

INHRR registration as applicable; Spanish-language labelling required by national law. Standard cold-chain conditions; logistical constraints typical of the contemporary Venezuelan economic environment.

Import/Export Rules

INHRR and Ministry of Popular Power for Productive Agriculture and Lands clearance for live invertebrates; CITES Appendix II paperwork for Hirudo medicinalis / verbana. International sanctions environment may further restrict commercial flows.

Reimbursement Context

Venezuelan public health system 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. The contemporary Venezuelan regulatory environment is challenging for any independent verification work; this entry should be treated as preliminary and confirmed with Venezuelan regulatory counsel before any operational use.

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.