Taiwan FDA registration b27fb6ddff5efd19b7fc607fb867f536
"LEICA" SURGIPATH Stain Reagent Kits (Non-Sterile)
TW: "錸卡" 瑟基帕司染色試劑組 (未滅菌)
Registration details
- Analysis ID
- b27fb6ddff5efd19b7fc607fb867f536
- License Form
- Ministry of Health Medical Device Import No. 013511
- Customs Code
- DHA09401351106
Company information
- Manufacturer
- LEICA BIOSYSTEMS RICHMOND INC.
- Manufacturer Country
- United States
- Authorized Representative
- ALL PROMISE ENTERPRISE INC.
Product details
- 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 18, 2013
- Expiry Date
- Oct 18, 2023
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "LEICA" SURGIPATH Stain Reagent Kits (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 b27fb6ddff5efd19b7fc607fb867f536 and manufactured by LEICA BIOSYSTEMS RICHMOND INC.. The authorized representative in Taiwan is ALL PROMISE ENTERPRISE INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices