Regulatory Authorisation

Verifiable, by name.

Aevivo Longevity operates under GÉNESE SOBRANCEIRA, LDA, an INFARMED-authorised medical device distributor in Portugal and a registered economic operator on the EU's EUDAMED database. Both registrations are public; both can be verified directly with the issuing authority.

Legal Entity

GÉNESE SOBRANCEIRA, LDA

Trading As

Aevivo Longevity

NIF (Tax ID)

519 331 800

Registered Office

Calçada da Ajuda 35, Bloco 5, r/c esq., 1300-006 Lisboa, Portugal

Jurisdiction

Portuguese limited liability company. Registered with the Portuguese Conservatória do Registo Comercial.

Medical Device Distributor · Portugal

INFARMED, I.P.

Certificate No.

3800/DM/2026

Issued By

Autoridade Nacional do Medicamento e Produtos de Saúde, I.P.

Scope

Authorised distributor of medical devices for human use, in compliance with EU MDR 2017/745.

Verify

infarmed.pt · certificate document on file with our regulatory team and shared with verified clinics on request.

EU Medical Device Operator Registry

EUDAMED

Status

Registered economic operator (importer / distributor of medical devices)

Database

EUDAMED (European Database on Medical Devices)

Verify

ec.europa.eu/tools/eudamed · search by entity name "Genese Sobranceira" or by Portuguese NIF.

For Verified Clinics

Documentation packs

Full INFARMED certificate, EUDAMED registration screenshot, sample Certificate of Analysis per peptide class, and supplier-side GMP documentation are shared with clinics that complete the practitioner application.

Apply for clinic access

Compliance posture. All Aevivo Longevity materials are For Research Use Only and supplied to licensed practitioners and qualified researchers. The receiving practitioner is solely responsible for compounding, prescription, and compliance with local regulation, including the EU Medicinal Products Regulation, the Medical Device Regulation (EU 2017/745), and any national-level rules where the practice is located.