Taiwan FDA registration acdd2f1816445f84f794c9f8920712ce
"Figon" ultra-light preterm infant central venous catheter
TW: “斐貢”超輕早產兒中央靜脈導管
Taiwan·Risk Class 2·VYGON·Registered Dec 23, 2008 – Dec 23, 2013CancelledRegistration details
- Analysis ID
- acdd2f1816445f84f794c9f8920712ce
- Customs Code
- DHA00601962308
Company information
- Manufacturer
- VYGON
- Manufacturer Country
- France
- Authorized Representative
- TRIPLE ROPES ENTERPRISE CO., LTD.
Product details
- Intended Use
- It is designed for very low birth weight prematures (VLBW) weighing less than 800 grams and can be visualized on X-ray. It is a polyureamine catheter inserted from a peripheral vein that can be administered and nourished for a long time.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Dec 23, 2008
- Expiry Date
- Dec 23, 2013
- Cancellation Date
- Apr 24, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Figon" ultra-light preterm infant central venous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number acdd2f1816445f84f794c9f8920712ce and manufactured by VYGON. The authorized representative in Taiwan is TRIPLE ROPES ENTERPRISE CO., LTD..
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