Taiwan FDA registration 460ab5f62d20e74a1451d920b303d6fc
"Hengyang" infusion set
TW: “恆漾”輸液器
Taiwan·Risk Class 2·NEEDLELESS CORPORATION·Registered Sep 19, 2019 – Apr 27, 2022CancelledRegistration details
- Analysis ID
- 460ab5f62d20e74a1451d920b303d6fc
Company information
- Manufacturer
- NEEDLELESS CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BEAUTY BRIGHT(B.B) COMPANY., 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.5440 血管內輸液套
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Sep 19, 2019
- Expiry Date
- Apr 27, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hengyang" infusion set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 460ab5f62d20e74a1451d920b303d6fc and manufactured by NEEDLELESS CORPORATION. The authorized representative in Taiwan is BEAUTY BRIGHT(B.B) COMPANY., LTD.
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