Taiwan FDA registration dabe09a32ea3cace93d361e7929f6123
EASYMAX Glucose Control Solutions (Non-Sterile)
TW: 宜瑪氏葡萄糖品管液(未滅菌)
Registration details
- Analysis ID
- dabe09a32ea3cace93d361e7929f6123
- License Form
- Ministry of Health Medical Device Manufacturing No. 008718
Company information
- Manufacturer
- EPS BIO TECHNOLOGY CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- EPS BIO TECHNOLOGY CORP.
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
- Dec 09, 2020
- Expiry Date
- Dec 09, 2025
About this record
Access comprehensive regulatory information for EASYMAX Glucose Control Solutions (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 dabe09a32ea3cace93d361e7929f6123 and manufactured by EPS BIO TECHNOLOGY CORP.. The authorized representative in Taiwan is EPS BIO TECHNOLOGY CORP..
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.
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