Tosama d.o.o.
Slovenian manufacturer of sanitary, medical, hygiene, baby, and private-label tampon products.
Tosama manufactures sanitary materials, medical supplies, tampons, sanitary pads, cotton products, wound-care items, baby products, and selected pet-care lines at its Vir pri Domzalah production site. The company positions itself as a major European private-label tampon producer and exports hygiene and medical products across Europe, the Americas, Asia, and Australia.
- Type
- Manufacturer
- Location
- Domzale, Slovenia
- Founded
- 1923
- Website
- tosama.si
- Categories
- Medical & Healthcare Supplies, Personal Care, Baby Care & Feeding, Pet Care & Accessories
- Markets
- Germany, Italy, United Kingdom, France, Sweden, United States, Canada, India, China, Colombia, Brazil, 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)