Ghetaldus Optika d.o.o.
为亚得里亚海地区供货的克罗地亚光学镜片和眼镜制造商。
Ghetaldus 在其萨格勒布工厂生产光学镜片、眼镜架和隐形眼镜。该公司成立于 1978 年，为克罗地亚和东南欧各地的眼镜商、眼镜零售连锁店和医疗设备分销商提供产品。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Zagreb, Croatia
- Founded
- 1978
- Website
- ghetaldus.hr
- Categories
- 眼镜和太阳镜, 医疗保健用品
- Markets
- 克罗地亚, 斯洛文尼亚, 波斯尼亚和黑塞哥维那, 塞尔维亚
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 2026-08-05 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- web-presence-since (green), checked 2026-08-05 Internet Archive (Wayback)
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- CE Marking EU NANDO (notified bodies)
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)