Taiwan FDA registration d496a5687c19205311581f3c9274b523
“Arthesys” Y-Connector
TW: “亞提斯” Y型連接器
Taiwan·Risk Class 2·MD·ARTHESYS·Registered Mar 19, 2021 – Mar 19, 2026ExpiredRegistration details
- Analysis ID
- d496a5687c19205311581f3c9274b523
- License Form
- Ministry of Health Medical Device Import No. 034464
- Customs Code
- DHA05603446407
Company information
- Manufacturer
- ARTHESYS
- Manufacturer Country
- France
- Authorized Representative
- CATHERINE CONSULTANTS 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)
- E4290 Arterial vascular bypass joint piston, multi-duct joint or accessory
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 19, 2021
- Expiry Date
- Mar 19, 2026
About this record
Access comprehensive regulatory information for “Arthesys” Y-Connector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d496a5687c19205311581f3c9274b523 and manufactured by ARTHESYS. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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