Taiwan FDA registration ff3fc4b4a66556fdcc22e752936753b8
“Covidien” Parietex Plug and patch system
TW: “柯惠”帕瑞得網塞式修補系統
Taiwan·Risk Class 2·MD·SOFRADIM PRODUCTION·Registered Nov 16, 2015 – Nov 16, 2020CancelledRegistration details
- Analysis ID
- ff3fc4b4a66556fdcc22e752936753b8
- License Form
- Ministry of Health Medical Device Import No. 027774
- Customs Code
- DHA05602777405
Company information
- Manufacturer
- SOFRADIM PRODUCTION
- Manufacturer Country
- France
- Authorized Representative
- Taiwan Covidien Corporation Limited
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I3300 Surgical mesh
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 16, 2015
- Expiry Date
- Nov 16, 2020
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for “Covidien” Parietex Plug and patch system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ff3fc4b4a66556fdcc22e752936753b8 and manufactured by SOFRADIM PRODUCTION. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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.
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