Taiwan FDA registration a1cc835edd749851945c24fed554ec71
Sergi General Purpose Reaction Reagent (Smear Fixative) (Unsterilized)
TW: 瑟吉一般目的之反應試劑(抹片固定液) (未滅菌)
Taiwan·Risk Class 1·SURGIPATH MEDICAL INDUSTRIES, INC.·Registered May 04, 2006 – May 04, 2016CancelledRegistration details
- Analysis ID
- a1cc835edd749851945c24fed554ec71
- Customs Code
- DHA04400435409
Company information
- Manufacturer
- SURGIPATH MEDICAL INDUSTRIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- FU SHING MEDICAL CO., LTD.
Product details
- 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
- May 04, 2006
- Expiry Date
- May 04, 2016
- Cancellation Date
- May 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Sergi General Purpose Reaction Reagent (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 a1cc835edd749851945c24fed554ec71 and manufactured by SURGIPATH MEDICAL INDUSTRIES, INC.. The authorized representative in Taiwan is FU SHING MEDICAL CO., LTD..
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