Taiwan FDA registration 36d118de02201b54ac7bba07af13f118
"DXN" a number of corrective products
TW: “德信”多項校正品
Taiwan·Risk Class 2·DIASYS DIAGNOSTIC SYSTEMS GMBH·Registered May 13, 2021 – May 13, 2026ExpiredRegistration details
- Analysis ID
- 36d118de02201b54ac7bba07af13f118
- Customs Code
- DHA05603465300
Company information
- Manufacturer
- DIASYS DIAGNOSTIC SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Used in optical colorimetric analysis systems, it can be used for multiple quantitative corrections.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- May 13, 2021
- Expiry Date
- May 13, 2026
About this record
Access comprehensive regulatory information for "DXN" a number of corrective products in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36d118de02201b54ac7bba07af13f118 and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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