Ghetaldus Optika d.o.o.
Adriyatik bölgesine ürün tedarik eden Hırvat optik lens ve gözlük üreticisi.
Ghetaldus, Zagreb'deki tesisinde optik lensler, oftalmik çerçeveler ve kontakt lensler üretmektedir. 1978 yılında kurulan şirket, Hırvatistan ve Güneydoğu Avrupa'da gözlükçülere, optik perakende zincirlerine ve tıbbi cihaz distribütörlerine ürün tedarik ediyor.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Zagreb, Croatia
- Founded
- 1978
- Website
- ghetaldus.hr
- Categories
- Gözlük ve Güneş Gözlüğü, Tıbbi ve Sağlık Malzemeleri
- Markets
- Hırvatistan, Slovenya, Bosna-Hersek, Sırbistan
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)