Taiwan FDA registration 6d2517b382a32986d4c0ef7ab450876e
DiaSys UIBC FS (Non-Sterile)
TW: 德賽不飽和鐵結合能力試劑 (未滅菌)
Taiwan·Risk Class 1·MD·DIASYS DIAGNOSTIC SYSTEMS GMBH·Registered Jul 31, 2020 – Jul 31, 2025ExpiredRegistration details
- Analysis ID
- 6d2517b382a32986d4c0ef7ab450876e
- License Form
- Ministry of Health Medical Device Import No. 021806
- Customs Code
- DHA09402180608
Company information
- Manufacturer
- DIASYS DIAGNOSTIC SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDITRUST MEDICAL SERVICE & CONSULTANT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Iron Binding Ability Test System (A.1415)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1415 Iron Binding Capacity Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 31, 2020
- Expiry Date
- Jul 31, 2025
About this record
Access comprehensive regulatory information for DiaSys UIBC FS (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 6d2517b382a32986d4c0ef7ab450876e and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is MEDITRUST MEDICAL SERVICE & CONSULTANT CO., LTD..
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