Taiwan FDA registration b674f09ca063c2cf02094f17f8826f74

KIWI SEPT CARE SOLUTION

TW: 金舒視雙氧液

Taiwan·Risk Class 2·MD·Taiyu Chemical Pharmaceutical Factory Co., Ltd·Registered Jan 16, 1996 – Jan 16, 2026Expired

Registration details

Analysis ID: b674f09ca063c2cf02094f17f8826f74
License Form: Department of Health Medical Device Manufacturing No. 000628
Customs Code: DHY00500062802

Company information

Manufacturer: Taiyu Chemical Pharmaceutical Factory Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: TAI YU CHEMICAL & PHARMACEUTICAL CO., LTD.

Product details

Intended Use: Performance changes: As detailed in Chinese copy of the imitation order (the original approved copy of the imitation label approved on July 5, 102 is withdrawn and invalidated).
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 16, 1996
Expiry Date: Jan 16, 2026

About this record

Access comprehensive regulatory information for KIWI SEPT CARE SOLUTION in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b674f09ca063c2cf02094f17f8826f74 and manufactured by Taiyu Chemical Pharmaceutical Factory Co., Ltd. The authorized representative in Taiwan is TAI YU CHEMICAL & PHARMACEUTICAL CO., LTD..

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