Taiwan FDA registration 12832865e295b8b03b70878a9f0eb140
“RI MING” Infusion set
TW: “笠民”輸液器
Taiwan·Risk Class 2·MD·NEEDLELESS CORPORATION·Registered Oct 20, 2020 – Apr 27, 2027ActiveRegistration details
- Analysis ID
- 12832865e295b8b03b70878a9f0eb140
- License Form
- Ministry of Health Medical Device Manufacturing No. 006979
Company information
- Manufacturer
- NEEDLELESS CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- RI-MING ENTERPRISES 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)
- J5440 Intravascular infusion sleeve
- Import Information
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- Oct 20, 2020
- Expiry Date
- Apr 27, 2027
About this record
Access comprehensive regulatory information for “RI MING” 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 12832865e295b8b03b70878a9f0eb140 and manufactured by NEEDLELESS CORPORATION. The authorized representative in Taiwan is RI-MING ENTERPRISES CO., LTD..
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