Taiwan FDA registration 8b80d04aaa4c6ea611832bbb3321361d
Sergipas smear fixative (unsterilized)
TW: 瑟吉帕斯抹片固定液(未滅菌)
Taiwan·Risk Class 1·SURGIPATH MEDICAL INDUSTRIES, INC.·Registered Jan 08, 2007 – Jan 08, 2017CancelledRegistration details
- Analysis ID
- 8b80d04aaa4c6ea611832bbb3321361d
- Customs Code
- DHA04400550305
Company information
- Manufacturer
- SURGIPATH MEDICAL INDUSTRIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- MIN JIER FIRM
Product details
- Intended Use
- Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.4010 Reaction Reagents for General Purposes
- Import Information
- import
Dates and status
- Registration Date
- Jan 08, 2007
- Expiry Date
- Jan 08, 2017
- Cancellation Date
- Dec 05, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Sergipas smear fixative (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8b80d04aaa4c6ea611832bbb3321361d and manufactured by SURGIPATH MEDICAL INDUSTRIES, INC.. The authorized representative in Taiwan is MIN JIER FIRM.
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