Taiwan FDA registration ec7eddf38c699dfc6295d60d334a075a

"Leison" Glucose Control Solution (Non-sterile)

TW: "連陞" 葡萄糖品管液 (未滅菌)

Taiwan·Risk Class 1·MD·LEISON BIOTECH CO., LTD.·Registered Apr 13, 2018 – Apr 13, 2028Active

Registration details

Analysis ID: ec7eddf38c699dfc6295d60d334a075a
License Form: Ministry of Health Medical Device Manufacturing No. 007215

Company information

Manufacturer: LEISON BIOTECH CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: LEISON BIOTECH CO., LTD.

Product details

Intended Use: Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1660 Quality Control Materials (Analytical and Non-Analytical)
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Apr 13, 2018
Expiry Date: Apr 13, 2028

About this record

Access comprehensive regulatory information for "Leison" Glucose Control 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 ec7eddf38c699dfc6295d60d334a075a and manufactured by LEISON BIOTECH CO., LTD.. The authorized representative in Taiwan is LEISON 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.