Taiwan FDA registration 50180a08483144a3d08c4473ece6499b
"Leica" Surgipath Stains Reagent Kit (Non-Sterile)
TW: "徠卡"瑟基帕思染色試劑組(未滅菌)
Taiwan·Risk Class 1·MD·LEICA BIOSYSTEMS RICHMOND INC.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 50180a08483144a3d08c4473ece6499b
- License Form
- Ministry of Health Medical Device Import Registration No. 010458
- Customs Code
- DHA08401045804
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 and pathology devices
- Product Type (Level 2)
- B1850 Dyes and chemical solution dyes
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "Leica" Surgipath Stains Reagent Kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 50180a08483144a3d08c4473ece6499b and manufactured by LEICA BIOSYSTEMS RICHMOND INC.. The authorized representative in Taiwan is BOND BIOTECH, INC..
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