Taiwan FDA registration 8632d5ca615b72bcc7bbd139da4de3ca
“E-WIRE” GUIDE WIRE
TW: “依外兒”引導線
Taiwan·Risk Class 2·MD·JOTEC GmbH·Registered Apr 24, 2015 – Apr 24, 2020CancelledRegistration details
- Analysis ID
- 8632d5ca615b72bcc7bbd139da4de3ca
- License Form
- Ministry of Health Medical Device Import No. 027273
- Customs Code
- DHA05602727309
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)
- E1330 Catheter Lead
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 24, 2015
- Expiry Date
- Apr 24, 2020
- 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-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 8632d5ca615b72bcc7bbd139da4de3ca and manufactured by JOTEC GmbH. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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