Taiwan FDA registration 4857a1e0dfc76e02eefb0d9066be3cee
“Imaxeon” MEDRAD Centargo Patient Line
TW: “益邁森” 輸液管套組
Taiwan·Risk Class 2·MD·IMAXEON PTY LTD.·Registered Mar 30, 2021 – Mar 30, 2026ExpiredRegistration details
- Analysis ID
- 4857a1e0dfc76e02eefb0d9066be3cee
- License Form
- Ministry of Health Medical Device Import No. 034479
- Customs Code
- DHA05603447907
Company information
- Manufacturer
- IMAXEON PTY LTD.
- Manufacturer Country
- Australia
- Authorized Representative
- HSIEN TAI INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1650 Vascular photography syringes and syringes
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 30, 2021
- Expiry Date
- Mar 30, 2026
About this record
Access comprehensive regulatory information for “Imaxeon” MEDRAD Centargo Patient Line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4857a1e0dfc76e02eefb0d9066be3cee and manufactured by IMAXEON PTY LTD.. The authorized representative in Taiwan is HSIEN TAI INSTRUMENTS CO., LTD..
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