Taiwan FDA registration 79b4483ac20437b67c969b3cf14f1d70
“Iradimed”3880 MRI Monitoring System
TW: “艾樂得”磁振造影生理監視系統
Taiwan·Risk Class 2·MD·Iradimed Corporation·Registered Jul 03, 2022 – Jul 03, 2027ActiveRegistration details
- Analysis ID
- 79b4483ac20437b67c969b3cf14f1d70
- License Form
- Ministry of Health Medical Device Import No. 035519
- Customs Code
- DHA05603551901
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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E2300 Cardiac Monitor (incl. Cardiac Counter and Heart Rate Alert)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 03, 2022
- Expiry Date
- Jul 03, 2027
About this record
Access comprehensive regulatory information for “Iradimed”3880 MRI Monitoring System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79b4483ac20437b67c969b3cf14f1d70 and manufactured by Iradimed Corporation. The authorized representative in Taiwan is HSIEN TAI INSTRUMENTS CO., LTD..
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