Taiwan FDA registration df2c956cbc635ccecc42008e0714850c
“Iradimed” MRidium MRI Infusion Sets
TW: “艾樂得” 輸液系統輸液套
Taiwan·Risk Class 2·MD·Iradimed Corporation·Registered Aug 08, 2022 – Aug 08, 2027ActiveRegistration details
- Analysis ID
- df2c956cbc635ccecc42008e0714850c
- License Form
- Ministry of Health Medical Device Import No. 035751
- Customs Code
- DHA05603575102
Company information
- Manufacturer
- Iradimed Corporation
- Manufacturer Country
- United States
- Authorized Representative
- HSIEN TAI INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Aug 08, 2022
- Expiry Date
- Aug 08, 2027
About this record
Access comprehensive regulatory information for “Iradimed” MRidium MRI Infusion Sets in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df2c956cbc635ccecc42008e0714850c and manufactured by Iradimed Corporation. The authorized representative in Taiwan is HSIEN TAI INSTRUMENTS CO., LTD..
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