Tosama d.o.o.
Fabricante esloveno de productos sanitarios, médicos, de higiene, para bebés y de tampones de marca privada.
Tosama fabrica materiales sanitarios, suministros médicos, tampones, toallas sanitarias, productos de algodón, artículos para el cuidado de heridas, productos para bebés y líneas seleccionadas para el cuidado de mascotas en su sitio de producción de Vir pri Domzalah. La empresa se posiciona como un importante productor europeo de tampones de marca blanca y exporta productos médicos y de higiene a toda Europa, América, Asia y Australia.
- Type
- brand seeking distribution
- Location
- Domzale, Slovenia
- Founded
- 1923
- Website
- tosama.si
- Categories
- Suministros médicos y sanitarios, Cuidado personal, Cuidado y alimentación del bebé, Cuidado y accesorios para mascotas
- Markets
- Alemania, Italia, Reino Unido, Francia, Suecia, Estados Unidos, Canadá, India, China, Colombia, Brasil, 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)