Novacel Optical
Французский производитель рецептурных офтальмологических линз, управляющий одним из крупнейших в Европе современных линз…
Французский производитель рецептурных офтальмологических линз, управляющий одной из крупнейших в Европе современных лабораторий по производству линз, обслуживающей рынки Франции, Бельгии и Швейцарии.
- Type
- brand seeking distribution
- Location
- Chateau-Thierry, France
- Founded
- 1958
- Website
- novacel-optical.com
- Categories
- Очки и солнцезащитные очки, Медицинские товары и расходники
- Markets
- Франция, Бельгия, Швейцария, Испания, Германия
Verified facts
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- facility-registered (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- registered-since (green), checked 2026-08-29 INSEE Sirene (annuaire-entreprises)
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- places-goods-on-market (green), checked 2026-08-30 Registre national des producteurs (ADEME/SYDEREP), France
- registry-id-verified (green), checked 2026-08-20 SIREN published in the company's own legal notice, confirmed in the French business register
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- registry-active-global (green), checked 2026-08-29 INSEE Sirene (annuaire-entreprises)
- domain-registered (green), checked 2026-08-26 Domain registry record
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
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)
- Sunglasses and protective eyewear are personal protective equipment in the EU: CE marking under Regulation (EU) 2016/425 is required. European Commission (PPE)