Taiwan FDA registration f4e146178249d6cb68afb8b865ef8fab
“ESSILOR” Trial Lens Set (Non-Sterile)
TW: “依視路” 試驗鏡片組 (未滅菌)
Taiwan·Risk Class 1·MD·OCULUS OPTIKGERATE GMBH·Registered Jul 27, 2020 – Jul 27, 2025ExpiredRegistration details
- Analysis ID
- f4e146178249d6cb68afb8b865ef8fab
- License Form
- Ministry of Health Medical Device Import No. 021786
- Customs Code
- DHA09402178602
Company information
- Manufacturer
- OCULUS OPTIKGERATE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ESSILOR-POLYLITE TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the ophthalmic test lens group (M.1405) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1405 Ophthalmic Test Lens Group
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 27, 2020
- Expiry Date
- Jul 27, 2025
About this record
Access comprehensive regulatory information for “ESSILOR” Trial Lens Set (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f4e146178249d6cb68afb8b865ef8fab and manufactured by OCULUS OPTIKGERATE GMBH. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..
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