Taiwan FDA registration 45e8b15415736810b7fa476d0ce11520
“Needleless” Extension Tube
TW: “尼得立斯”延長管
Taiwan·Risk Class 2·MD·NEEDLELESS CORPORATION·Registered Dec 15, 2016 – Dec 15, 2026ActiveRegistration details
- Analysis ID
- 45e8b15415736810b7fa476d0ce11520
- License Form
- Ministry of Health Medical Device Manufacturing No. 005482
Company information
- Manufacturer
- NEEDLELESS CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- NEEDLELESS CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order. The indication was changed to: as detailed as Chinese the approved copy of the imitation order (the original approved copy of the imitation label approved on December 26, 105 is invalid).
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5440 Intravascular infusion sleeve
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 15, 2016
- Expiry Date
- Dec 15, 2026
About this record
Access comprehensive regulatory information for “Needleless” Extension Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 45e8b15415736810b7fa476d0ce11520 and manufactured by NEEDLELESS CORPORATION. The authorized representative in Taiwan is NEEDLELESS CORPORATION.
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