Taiwan FDA registration 8b6fb48c71285fc7bd62fe29aa98a020

"BaSO" MIF Stain Solution (Non-Sterile)

TW: "貝索" 阿米巴染色固定液 (未滅菌)

Taiwan·Risk Class 1·MD·BASO BIOTECH CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2026Active

Registration details

Analysis ID: 8b6fb48c71285fc7bd62fe29aa98a020
License Form: Ministry of Health Medical Device Manufacturing Registration No. 006244

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" MIF Stain Solution (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 8b6fb48c71285fc7bd62fe29aa98a020 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.