Taiwan FDA registration 92dc25b3542aa2650c53a5aeb1828366

SOCLEAN Buffer Saline Solution

TW: 舒麗淨無汞生理緩衝液

Taiwan·Risk Class 2·MD·NANG KUANG PHARMACEUTICAL CO., LTD.·Registered Jan 17, 2017 – Aug 16, 2024Expired

Registration details

Analysis ID: 92dc25b3542aa2650c53a5aeb1828366
License Form: Ministry of Health Medical Device Manufacturing No. 005646

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 Ophthalmic devices
Product Type (Level 2): M5928 Flexible Contact Lens Preservation
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Jan 17, 2017
Expiry Date: Aug 16, 2024

About this record

Access comprehensive regulatory information for SOCLEAN Buffer Saline Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 92dc25b3542aa2650c53a5aeb1828366 and manufactured by NANG KUANG PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is NANG KUANG PHARMACEUTICAL CO., LTD..

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