Taiwan FDA registration 177d64046c82e5c82c4b44f50dbdd800
Badi Iron D-Dimer Test-Quality Fluid
TW: 巴迪鐵克 D-二聚體檢驗試劑-品管液
Taiwan·Risk Class 2·Boditech Med Inc.·Registered Dec 04, 2024 – Dec 04, 2029ActiveRegistration details
- Analysis ID
- 177d64046c82e5c82c4b44f50dbdd800
- Customs Code
- DHA05603752006
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 quality control of D-dimer testing reagents manufactured/supplied by Boditech Med Inc.
- 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
- Dec 04, 2024
- Expiry Date
- Dec 04, 2029
About this record
Access comprehensive regulatory information for Badi Iron D-Dimer Test-Quality Fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 177d64046c82e5c82c4b44f50dbdd800 and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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