Taiwan FDA registration 1d5ee99707a38aaef6f741cd91fbd9a1
“BD” Q-Syte Luer Access Site Extension Sets
TW: “必帝”延長型無針式輸液套接頭。“BD”延長型無針式輸液套接頭。
Taiwan·Risk Class 2·MD·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Registered Sep 25, 2008 – Sep 25, 2028ActiveRegistration details
- Analysis ID
- 1d5ee99707a38aaef6f741cd91fbd9a1
- License Form
- Department of Health Medical Device Import No. 019235
- Customs Code
- DHA00601923502
Company information
- Manufacturer
- BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.
- Manufacturer Country
- United States
- Authorized Representative
- BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE)
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)
- J5440 Intravascular infusion sleeve
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 25, 2008
- Expiry Date
- Sep 25, 2028
About this record
Access comprehensive regulatory information for “BD” Q-Syte Luer Access Site Extension Sets in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1d5ee99707a38aaef6f741cd91fbd9a1 and manufactured by BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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