SWEDEN & MARTINA S.P.A.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Due Carrare Padova, Italy
- Categories
- Стоматологические материалы и оборудование
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- fda-registered (green), checked 2026-08-26 FDA
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- export-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- workforce-on-record (green), checked 2026-08-25 OpenCoesione (opencoesione.gov.it), open data on project subjects
- listed-in-registry (amber), checked 2026-08-26 BRIS, EU business registers interconnection (e-justice.europa.eu)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Import rules for these goods
- 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)