Taiwan FDA registration e71a43024cec923d26e3ea85f52f7a62
"BaSO" Diff-Quik Stain Set (Non-Sterile)
TW: "貝索" 快速染色試劑組(未滅菌)
Registration details
- Analysis ID
- e71a43024cec923d26e3ea85f52f7a62
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 006358
Company information
- Manufacturer
- BASO BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BASO BIOTECH CO., LTD.
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
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "BaSO" Diff-Quik Stain Set (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 e71a43024cec923d26e3ea85f52f7a62 and manufactured by BASO BIOTECH CO., LTD.. The authorized representative in Taiwan is BASO BIOTECH CO., LTD..
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