Kerecis
Kerecis produkuje produkty do opatrywania ran na bazie rybiej skóry dla gotowych do eksportu kanałów B2B.
Kerecis produkuje w Isafjordur produkty do opatrywania ran, wyroby medyczne i produkty z tkanki regeneracyjnej na bazie rybiej skóry. Założona w 2009 roku firma zaopatruje szpitale, kliniki leczenia ran, dystrybutorów produktów medycznych i rynki eksportowe w IS, NO, DK, USA i powiązanych rynkach eksportowych.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Isafjordur, Iceland
- Founded
- 2009
- Website
- kerecis.com
- Categories
- Artykuły medyczne i związane z opieką zdrowotną
- Markets
- Islandia, Norwegia, Dania, Stany Zjednoczone
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
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- debarment-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- fda-registered (green), checked 2026-08-08 FDA
- sanctions-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- domain-registered (green), checked 2026-08-08 Domain registry 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)