Tosama d.o.o.
Produttore sloveno di prodotti sanitari, medici, igienici, per bambini e assorbenti con marchio del distributore.
Tosama produce materiali sanitari, forniture mediche, tamponi, assorbenti, prodotti in cotone, articoli per la cura delle ferite, prodotti per bambini e linee selezionate per la cura degli animali domestici nel suo sito produttivo di Vir pri Domzalah. L'azienda si posiziona come uno dei principali produttori europei di tamponi a marchio privato ed esporta prodotti igienici e medici in tutta Europa, nelle Americhe, in Asia e in Australia.
- Type
- brand seeking distribution
- Location
- Domzale, Slovenia
- Founded
- 1923
- Website
- tosama.si
- Categories
- Forniture medicali e sanitarie, Cura della persona, Cura e alimentazione del bambino, Cura e accessori per animali
- Markets
- Germania, Italia, Regno Unito, Francia, Svezia, Stati Uniti, Canada, India, Cina, Colombia, Brasile, Australia
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-10 Mail server of the company domain
- debarment-clear (green), checked 2026-08-10 OpenSanctions
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- domain-registered (green), checked 2026-08-02 Domain registry record
- facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
- fda-registered (green), checked 2026-08-10 FDA
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- BRCGS Certification BRCGS Directory
- FDA Registered FDA Establishment Registration
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)