Keeler Ltd.
英国に拠点を置く眼科用光学設計および製造会社で、世界中の診断機器を製造しています。
英国に拠点を置く眼科用光学設計および製造会社で、米国、オーストラリア、インドの市場向けに診断機器、ルーペ、検眼機器を製造しています。
- Type
- Manufacturer
- Location
- Windsor, United Kingdom
- Founded
- 1917
- Website
- keelerglobal.com
- Categories
- 医療およびヘルスケア用品, メガネとサングラス
- Markets
- イギリス, アメリカ合衆国, オーストラリア, インド, ドイツ
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- ch-active (green), checked 2026-06-20 Companies House
- registered-manufacturer (green), checked 2026-06-20 Companies House
- directors-on-file (green), checked 2026-06-20 Companies House
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality 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)