Taiwan FDA registration 5f9c479a3bc7e572e08da2ed34c7d212
“Iradimed” MRidium MRI Infusion Pump and Pulse Oximeter System
TW: “艾樂得” 輸液系統
Taiwan·Risk Class 2·MD·Iradimed Corporation·Registered Aug 08, 2022 – Aug 08, 2027ActiveRegistration details
- Analysis ID
- 5f9c479a3bc7e572e08da2ed34c7d212
- License Form
- Ministry of Health Medical Device Import No. 035550
- Customs Code
- DHA05603555005
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)
- J5725 Infusion pump
- 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 Pump and Pulse Oximeter System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5f9c479a3bc7e572e08da2ed34c7d212 and manufactured by Iradimed Corporation. The authorized representative in Taiwan is HSIEN TAI INSTRUMENTS CO., LTD..
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