Taiwan FDA registration d0b87316639712db2eb11237ff5e7280
"Yangpu" single-use venous blood collection needle
TW: “陽普”一次性使用靜脈採血針
Taiwan·Risk Class 2·GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.·Registered Oct 24, 2016 – Oct 24, 2026ActiveRegistration details
- Analysis ID
- d0b87316639712db2eb11237ff5e7280
- Customs Code
- DHA09200077901
Company information
- Manufacturer
- GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- BEAM INTERNATIONAL INC.
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
- Input;; Chinese goods
Dates and status
- Registration Date
- Oct 24, 2016
- Expiry Date
- Oct 24, 2026
About this record
Access comprehensive regulatory information for "Yangpu" single-use venous blood collection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d0b87316639712db2eb11237ff5e7280 and manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..
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