Taiwan FDA registration e50bb837fd539ba0feb0909b6aa00250
“Jotec” E-wire Guide Wire
TW: “優德克” 伊旺導引線
Taiwan·Risk Class 2·MD·JOTEC GmbH·Registered Feb 23, 2021 – Feb 23, 2026ExpiredRegistration details
- Analysis ID
- e50bb837fd539ba0feb0909b6aa00250
- License Form
- Ministry of Health Medical Device Import No. 034340
- Customs Code
- DHA05603434002
Company information
- Manufacturer
- JOTEC GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- EMERGO TAIWAN LIMITED
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)
- E1330 Catheter Lead
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 23, 2021
- Expiry Date
- Feb 23, 2026
About this record
Access comprehensive regulatory information for “Jotec” E-wire Guide Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e50bb837fd539ba0feb0909b6aa00250 and manufactured by JOTEC GmbH. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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