Taiwan FDA registration 17a00b57f055f613090090c189cf3471
Miacare clarion multi-purpose solution
TW: 美若康睛透多效保養液
Taiwan·Risk Class 2·MD·NANG KUANG PHARMACEUTICAL CO., LTD.·Registered Nov 10, 2016 – Oct 12, 2025ExpiredRegistration details
- Analysis ID
- 17a00b57f055f613090090c189cf3471
- License Form
- Ministry of Health Medical Device Manufacturing No. 005539
Company information
- Manufacturer
- NANG KUANG PHARMACEUTICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BENQ MATERIALS CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5928 Flexible Contact Lens Preservation
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 10, 2016
- Expiry Date
- Oct 12, 2025
About this record
Access comprehensive regulatory information for Miacare clarion multi-purpose solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17a00b57f055f613090090c189cf3471 and manufactured by NANG KUANG PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is BENQ MATERIALS CORP..
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