Taiwan FDA registration de88a138edba42fe515c6c70b6bf7c1a
Anki physiological buffer
TW: 杏輝生理緩衝液
Taiwan·Risk Class 2·SINPHAR PHARMACEUTICAL CO., LTD.·Registered May 09, 2001 – May 09, 2016CancelledRegistration details
- Analysis ID
- de88a138edba42fe515c6c70b6bf7c1a
- Customs Code
- DHY00500090209
Company information
- Manufacturer
- SINPHAR PHARMACEUTICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SINPHAR PHARMACEUTICAL CO., LTD.
Product details
- Product Type (Level 1)
- M000 Ophthalmology
- Import Information
- Domestic
Dates and status
- Registration Date
- May 09, 2001
- Expiry Date
- May 09, 2016
- Cancellation Date
- Nov 07, 2016
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Anki 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 de88a138edba42fe515c6c70b6bf7c1a and manufactured by SINPHAR PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is SINPHAR PHARMACEUTICAL CO., LTD..
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