Taiwan FDA registration 730b3863a639de6076b918491b264be1
"Hokichi" hemolysate (unsterilized)
TW: “保吉”血球溶解液 (未滅菌)
Taiwan·Risk Class 1·HOLOGIC, INC.·Registered Jun 21, 2012 – Jun 21, 2022CancelledRegistration details
- Analysis ID
- 730b3863a639de6076b918491b264be1
- Customs Code
- DHA04401185904
Company information
- Manufacturer
- HOLOGIC, INC.
- Manufacturer Country
- United States
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of red blood cell dissolving agent (B.8540) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.8540 紅血球溶解劑
- Import Information
- import
Dates and status
- Registration Date
- Jun 21, 2012
- Expiry Date
- Jun 21, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hokichi" hemolysate (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 730b3863a639de6076b918491b264be1 and manufactured by HOLOGIC, INC.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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