Taiwan FDA registration f98ddaf18096aebd8e0bac69df8a7162
Desai. Iron liquid kit (unsterilized)
TW: 德賽. 鐵液體試劑盒(未滅菌)
Taiwan·Risk Class 1·DIASYS DIAGNOSTIC SYSTEMS GMBH·Registered Feb 03, 2006 – Feb 03, 2026ExpiredRegistration details
- Analysis ID
- f98ddaf18096aebd8e0bac69df8a7162
- Customs Code
- DHA04400257400
Company information
- Manufacturer
- DIASYS DIAGNOSTIC SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDITRUST MEDICAL SERVICE & CONSULTANT CO., LTD.
Product details
- Intended Use
- For in vitro quantitative determination of human serum iron.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1410 Iron (non-blood matrix) testing system
- Import Information
- import
Dates and status
- Registration Date
- Feb 03, 2006
- Expiry Date
- Feb 03, 2026
About this record
Access comprehensive regulatory information for Desai. Iron liquid kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f98ddaf18096aebd8e0bac69df8a7162 and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is MEDITRUST MEDICAL SERVICE & CONSULTANT CO., LTD..
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