Taiwan FDA registration 898c2959afeeb54bdb481356b1ce4b41
EV Single-use Containers for Human Venous Blood Specimen Collection(Sterile Glucose Tube)
TW: 醫凡一次性使用非真空採血管(氟化鈉/K2 EDTA)
Taiwan·Risk Class 2·MD·HEBEI XINLE SCI & TECH CO., LTD.·Registered Apr 30, 2014 – Apr 30, 2024ExpiredRegistration details
- Analysis ID
- 898c2959afeeb54bdb481356b1ce4b41
- License Form
- Ministry of Health Medical Device Land Transport No. 000527
- Customs Code
- DHA09200052700
Company information
- Manufacturer
- HEBEI XINLE SCI & TECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- AGREE HEALTH CARE TECHNOLOGY, LTD.
Product details
- Intended Use
- This product is intended for blood glucose testing.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1675 Blood Sample Collection Device
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Apr 30, 2014
- Expiry Date
- Apr 30, 2024
About this record
Access comprehensive regulatory information for EV Single-use Containers for Human Venous Blood Specimen Collection(Sterile Glucose Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 898c2959afeeb54bdb481356b1ce4b41 and manufactured by HEBEI XINLE SCI & TECH CO., LTD.. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, LTD..
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