Ghetaldus Optika d.o.o.
アドリア海地域に製品を供給するクロアチアの光学レンズとアイウェアのメーカー。
Ghetaldus は、ザグレブの施設で光学レンズ、眼鏡フレーム、コンタクト レンズを製造しています。 1978 年に設立された同社は、クロアチアおよび南東ヨーロッパ全域で眼鏡店、眼鏡小売チェーン、医療機器販売業者に商品を提供しています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Zagreb, Croatia
- Founded
- 1978
- Website
- ghetaldus.hr
- Categories
- メガネとサングラス, 医療およびヘルスケア用品
- Markets
- クロアチア, スロベニア, ボスニア・ヘルツェゴビナ, セルビア
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)