Taiwan FDA registration 05b4d3e0951ef18ad7a52ed953b874a5
“E-VITA” OPEN PLUS STENT GRAFT SYSTEM
TW: “依威達”開放加強式血管支架系統
Taiwan·Risk Class 3·MD·JOTEC GmbH·Registered Dec 10, 2014 – Dec 10, 2019CancelledRegistration details
- Analysis ID
- 05b4d3e0951ef18ad7a52ed953b874a5
- License Form
- Ministry of Health Medical Device Import No. 026306
- Customs Code
- DHA05602630606
Company information
- Manufacturer
- JOTEC GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- LEIN YIH MEDICAL CO.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 10, 2014
- Expiry Date
- Dec 10, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “E-VITA” OPEN PLUS STENT GRAFT SYSTEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 05b4d3e0951ef18ad7a52ed953b874a5 and manufactured by JOTEC GmbH. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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