Single-use vacuum blood collection (separating gel/coagulant)
Taiwan·Risk Class 2·HEBEI XINLE SCI & TECH CO., LTD.·Registered Nov 30, 2018 – Nov 30, 2028Active- Analysis ID
- d48689da4ca21acb897498b5689ccb5a
- Customs Code
- DHA09200099109
- Manufacturer
- HEBEI XINLE SCI & TECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- EAFAN ENTERPRISE CO., LTD.
- Intended Use
- This product is used to take and collect blood for serum biochemical testing.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1675 Blood collection equipment
- Import Information
- Input;; Chinese goods
- Registration Date
- Nov 30, 2018
- Expiry Date
- Nov 30, 2028
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Access comprehensive regulatory information for Single-use vacuum blood collection (separating gel/coagulant) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d48689da4ca21acb897498b5689ccb5a and manufactured by HEBEI XINLE SCI & TECH CO., LTD.. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD, HEBEI XINLE SCI&TECH CO., LTD., and 2 recent registrations in the same category. 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.