Taiwan FDA registration 0f56292060cd240eb270d1c9361fdfad
“Aurum” Blood Glucose Control Solution(Non-Sterile)
TW: “瑞瑩”血糖品管液(未滅菌)
Registration details
- Analysis ID
- 0f56292060cd240eb270d1c9361fdfad
- License Form
- Ministry of Health Medical Device Manufacturing No. 009285
Company information
- Manufacturer
- AURUM BIOMEDICAL TECHNOLOGY, INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- AURUM BIOMEDICAL TECHNOLOGY, INC.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
- 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
- Sep 02, 2021
- Expiry Date
- Sep 02, 2026
About this record
Access comprehensive regulatory information for “Aurum” Blood 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 0f56292060cd240eb270d1c9361fdfad and manufactured by AURUM BIOMEDICAL TECHNOLOGY, INC.. The authorized representative in Taiwan is AURUM BIOMEDICAL TECHNOLOGY, INC..
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