Taiwan FDA registration dde9c430f61675ea9fa9d11f11ba99a9
Badiek Rotavirus Test Reagent – Tube Fluid
TW: 巴迪鐵克輪狀病毒檢驗試劑–品管液
Taiwan·Risk Class 2·Boditech Med Inc.·Registered Jul 13, 2022 – Jul 13, 2027ActiveRegistration details
- Analysis ID
- dde9c430f61675ea9fa9d11f11ba99a9
- Customs Code
- DHA05603567601
Company information
- Manufacturer
- Boditech Med Inc.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MEDRICH INSTRUMENT CO., LTD.
Product details
- Intended Use
- This product is used for in vitro diagnostic use for quality management of rotavirus test reagents.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jul 13, 2022
- Expiry Date
- Jul 13, 2027
About this record
Access comprehensive regulatory information for Badiek Rotavirus Test Reagent – Tube Fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dde9c430f61675ea9fa9d11f11ba99a9 and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
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