Taiwan FDA registration e12dd0c5f73fb12df72e65c8dfd11231
"Yifan" uses intravenous blood collection needles at a single time
TW: “醫凡”一次性使用靜脈採血針
Taiwan·Risk Class 2·HEBEI XINLE SCI & TECH CO., LTD.·Registered Jan 07, 2020 – Jan 07, 2025ExpiredRegistration details
- Analysis ID
- e12dd0c5f73fb12df72e65c8dfd11231
- Customs Code
- DHA09200110005
Company information
- Manufacturer
- HEBEI XINLE SCI & TECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- EAFAN ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5570 Subcutaneous single-chamber needle
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jan 07, 2020
- Expiry Date
- Jan 07, 2025
About this record
Access comprehensive regulatory information for "Yifan" uses intravenous blood collection needles at a single time in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e12dd0c5f73fb12df72e65c8dfd11231 and manufactured by HEBEI XINLE SCI & TECH CO., LTD.. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..
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