Taiwan FDA registration 8e900a3156a3962da6c147c56ae452fe
"Japan to Fuen" Aislit Il lead
TW: “日本來富恩”艾斯利特伊爾導引線
Taiwan·Risk Class 2·JAPAN LIFELINE CO., LTD.;; Japan Lifeline Co., Ltd. Toda Factory·Registered Nov 24, 2011 – Nov 24, 2021CancelledRegistration details
- Analysis ID
- 8e900a3156a3962da6c147c56ae452fe
- Customs Code
- DHA00602293409
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- ZENITH INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1330 Catheter Guide Wires
- Import Information
- import
Dates and status
- Registration Date
- Nov 24, 2011
- Expiry Date
- Nov 24, 2021
- Cancellation Date
- Aug 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Japan to Fuen" Aislit Il lead in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8e900a3156a3962da6c147c56ae452fe and manufactured by JAPAN LIFELINE CO., LTD.;; Japan Lifeline Co., Ltd. Toda Factory. The authorized representative in Taiwan is ZENITH INC..
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