Taiwan FDA registration 83e0a8245a157e4080c348c499fefb6f
AndoCor Flex Line Two Stage Venous Catheter
TW: 恩多寇福列克斯兩段式靜脈導管
Taiwan·Risk Class 2·MD·ANDOCOR NV·Registered Jan 16, 2019 – Jan 16, 2024ExpiredRegistration details
- Analysis ID
- 83e0a8245a157e4080c348c499fefb6f
- License Form
- Ministry of Health Medical Device Import No. 032073
- Customs Code
- DHA05603207308
Company information
- Manufacturer
- ANDOCOR NV
- Manufacturer Country
- Belgium
- Authorized Representative
- LEIN YIH MEDICAL CO.
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)
- E1300 catheter cannula
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 16, 2019
- Expiry Date
- Jan 16, 2024
About this record
Access comprehensive regulatory information for AndoCor Flex Line Two Stage 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 83e0a8245a157e4080c348c499fefb6f and manufactured by ANDOCOR NV. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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