"MASTELLI S.R.L."
Mastelli Bio-Pharmaceutical Workshop - Sanremo, Italy
Mastelli srl produces and distributes drugs, medical devices, cosmetics and pharmacologically active raw material "Polydeoxyribonucleotide".
- Type
- Manufacturer
- Location
- Sanremo, Italy
- Website
- https://mastelli.it
- Categories
- Fabricação farmacêutica, Suprimentos médicos e de saúde, Cuidados com a pele e cosméticos
Listed in a source registry
Italian public registries (Ministero della Salute / ANAC), domain proven by VAT on site
Verified facts
- state-aid-sector (green), checked 2026-07-13 Registro Nazionale degli Aiuti di Stato (rna.gov.it), open data
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- facility-registered (green), checked 2026-08-15 Ministero della Salute, stabilimenti riconosciuti (Reg. CE 853/2004)
- gmp-certified (green), checked 2026-02-20 EudraGMDP, EU register of GMP certificates (EMA)
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- vat-valid (green), checked 2026-08-12 VIES (European Commission)
Claimed certifications
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)