Taiwan FDA registration 496f1a9f083864283dff341809356736
"Leica" Serki Path staining kit (unsterilized)
TW: "徠卡"瑟基帕思染色試劑組(未滅菌)
Taiwan·Risk Class 1·LEICA BIOSYSTEMS RICHMOND INC.·Registered Jun 09, 2011 – Jun 09, 2026CancelledRegistration details
- Analysis ID
- 496f1a9f083864283dff341809356736
- Customs Code
- DHA04401045807
Company information
- Manufacturer
- LEICA BIOSYSTEMS RICHMOND INC.
- Manufacturer Country
- United States
- Authorized Representative
- BOND BIOTECH, INC.
Product details
- Intended Use
- Limited to the first grade identification range of dyes and chemical solution dyes (B.1850) of the management measures for medical devices.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.1850 Dyes and dyes for chemical solutions
- Import Information
- import
Dates and status
- Registration Date
- Jun 09, 2011
- Expiry Date
- Jun 09, 2026
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Leica" Serki Path staining kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 496f1a9f083864283dff341809356736 and manufactured by LEICA BIOSYSTEMS RICHMOND INC.. The authorized representative in Taiwan is BOND BIOTECH, INC..
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