Taiwan FDA registration 585f52494ed02035aebf175040a3a802
“OCULUS” Ophthalmic Trial Lens Set (Non-Sterile)
TW: “歐克勒斯”眼科試驗鏡片組 (未滅菌)
Taiwan·Risk Class 1·MD·OCULUS OPTIKGERATE GMBH·Registered Dec 05, 2019 – Dec 05, 2024ExpiredRegistration details
- Analysis ID
- 585f52494ed02035aebf175040a3a802
- License Form
- Ministry of Health Medical Device Import No. 021074
- Customs Code
- DHA09402107406
Company information
- Manufacturer
- OCULUS OPTIKGERATE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Carl Zeiss Co., Ltd. Taipei Branch
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
- Dec 05, 2019
- Expiry Date
- Dec 05, 2024
About this record
Access comprehensive regulatory information for “OCULUS” Ophthalmic 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 585f52494ed02035aebf175040a3a802 and manufactured by OCULUS OPTIKGERATE GMBH. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.
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