Taiwan FDA registration ddffefdfd1b713f0f63ea38a1e3ca0b4
"Nanguang" flush net mercury-free physiological buffer
TW: “南光”沖立淨無汞生理緩衝液
Taiwan·Risk Class 2·NANG KUANG PHARMACEUTICAL CO., LTD.·Registered Aug 01, 2011 – Aug 16, 2029ActiveRegistration details
- Analysis ID
- ddffefdfd1b713f0f63ea38a1e3ca0b4
- Customs Code
- DHY00500335304
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
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 01, 2011
- Expiry Date
- Aug 16, 2029
About this record
Access comprehensive regulatory information for "Nanguang" flush net mercury-free physiological buffer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ddffefdfd1b713f0f63ea38a1e3ca0b4 and manufactured by NANG KUANG PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is NANG KUANG PHARMACEUTICAL CO., LTD..
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