Taiwan FDA registration 6d6b4cba8214eb739120a7d0440bc447
A central venous catheter is introduced around the "Figon"
TW: “斐貢”周邊導入中央靜脈導管
Registration details
- Analysis ID
- 6d6b4cba8214eb739120a7d0440bc447
- Customs Code
- DHA00602474503
Company information
- Manufacturer
- Vygon GmbH & Co. KG
- Manufacturer Country
- Germany
- Authorized Representative
- MING HWAY TRADING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5200 Endovascular catheters
- Import Information
- import
Dates and status
- Registration Date
- Feb 21, 2013
- Expiry Date
- Feb 21, 2028
About this record
Access comprehensive regulatory information for A central venous catheter is introduced around the "Figon" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6d6b4cba8214eb739120a7d0440bc447 and manufactured by Vygon GmbH & Co. KG. The authorized representative in Taiwan is MING HWAY TRADING CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices