Taiwan FDA registration 5579f9b622af027bdd014d7b5d899575
Diken Vision Multi-Action Maintenance Solution
TW: 帝康視潤多效保養液
Taiwan·Risk Class 2·NANG KUANG PHARMACEUTICAL CO., LTD.·Registered Aug 06, 2020 – Oct 31, 2029ActiveRegistration details
- Analysis ID
- 5579f9b622af027bdd014d7b5d899575
Company information
- Manufacturer
- NANG KUANG PHARMACEUTICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- NANG KUANG PHARMACEUTICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.5928 Products for the preservation of soft contact lenses;; M.5918 Rigid Breathable Contact Lens Preservation Products
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 06, 2020
- Expiry Date
- Oct 31, 2029
About this record
Access comprehensive regulatory information for Diken Vision Multi-Action Maintenance Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5579f9b622af027bdd014d7b5d899575 and manufactured by NANG KUANG PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is NANG KUANG PHARMACEUTICAL CO., LTD..
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