Taiwan FDA registration 03f53c0d24840350d4a21e33e5bd1349
“Nipro” Surefuser+
TW: “尼普洛”微量輸液器
Taiwan·Risk Class 2·MD·Nipro Corporation Odate Factory·Registered Apr 17, 2014 – Apr 17, 2024ExpiredRegistration details
- Analysis ID
- 03f53c0d24840350d4a21e33e5bd1349
- License Form
- Ministry of Health Medical Device Import No. 026107
- Customs Code
- DHA05602610700
Company information
- Manufacturer
- Nipro Corporation Odate Factory
- Manufacturer Country
- Japan
- Authorized Representative
- HUA CHIANG MEDICAL 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
- Imported from abroad
Dates and status
- Registration Date
- Apr 17, 2014
- Expiry Date
- Apr 17, 2024
About this record
Access comprehensive regulatory information for “Nipro” Surefuser+ in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03f53c0d24840350d4a21e33e5bd1349 and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..
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