Taiwan FDA registration 157627b0cfa207364286ae45a7b0fb59
“Jotec”E-vita OPEN NEO
TW: “優德克”伊維塔開放式血管支架系統
Taiwan·Risk Class 3·MD·Jotec GmbH·Registered Sep 05, 2022 – Sep 05, 2027ActiveRegistration details
- Analysis ID
- 157627b0cfa207364286ae45a7b0fb59
- License Form
- Ministry of Health Medical Device Import No. 034623
- Customs Code
- DHA05603462301
Company information
- Manufacturer
- Jotec GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 05, 2022
- Expiry Date
- Sep 05, 2027
About this record
Access comprehensive regulatory information for “Jotec”E-vita OPEN NEO in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 157627b0cfa207364286ae45a7b0fb59 and manufactured by Jotec GmbH. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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