Taiwan FDA registration 302219c48001691472d69ee6d96028de
"Oke Road" myopia analyzer
TW: “歐克路” 近視分析儀
Taiwan·Risk Class 2·OCULUS OPTIKGERÄTE GMBH·Registered Jun 18, 2021 – Jun 18, 2026ExpiredRegistration details
- Analysis ID
- 302219c48001691472d69ee6d96028de
- Customs Code
- DHA05603473502
Company information
- Manufacturer
- OCULUS OPTIKGERÄTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TAIWAN HWA IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1350 角膜鏡;; M.1760 自動眼科驗光機;; M.1450 角膜弧度量測器
- Import Information
- import
Dates and status
- Registration Date
- Jun 18, 2021
- Expiry Date
- Jun 18, 2026
About this record
Access comprehensive regulatory information for "Oke Road" myopia analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 302219c48001691472d69ee6d96028de and manufactured by OCULUS OPTIKGERÄTE GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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