MOSS ORTOPEDISK KLINIKK AS
Ортопедическая клиника в Моссе | Ортопедическая клиника Мосса | Ортопедия Осло
Ортопедическая клиника, которая измеряет, адаптирует и ремонтирует ортопедические приспособления, такие как стельки, обувь, ортезы и протезы, а также приспособления для диабетической стопы, занятия спортом и активный отдых в Моссе, Осло, Вестби, Дробаке, Фолло.
- Type
- brand seeking distribution
- Location
- Moss, Norway
- Founded
- 2011
- Website
- https://www.moss-ok.no
- Categories
- Медицинские товары и расходники
Listed in a source registry
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
- domain-registered (green), checked 2026-08-03 Domain registry record
- sanctions-clear (green), checked 2026-08-03 OpenSanctions
- debarment-clear (green), checked 2026-08-03 OpenSanctions
- registry-activity (green), checked 2026-08-23 Norway Brønnøysund Register Centre (open bulk file)
- registry-active-global (green), checked 2026-08-23 Norway Brønnøysund Register Centre (open bulk file)
- tax-filing-active (green), checked 2026-08-23 Norway Brønnøysund Register Centre (open bulk file)
- workforce-on-record (green), checked 2026-08-23 Norway Brønnøysund Register Centre (open bulk file)
- leadership-on-record (green), checked 2026-08-03 Brønnøysund (roller)
- annual-accounts-filed (green), checked 2026-08-03 Regnskapsregisteret (Brønnøysund)
- registry-id-verified (green), checked 2026-07-11 Bronnoysund Register Centre, Central Coordinating Register of Legal Entities (Enhetsregisteret)
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)