Taiwan FDA registration 69abf7c654a5cd724117f1b9e1ab069e
"Japan Lai Fuen" Fix fixed bent electrode catheter
TW: “日本來富恩”菲克斯固定彎電極導管
Taiwan·Risk Class 2·JAPAN LIFELINE CO., LTD.;; Japan Lifeline Co., Ltd. Toda Factory·Registered Nov 23, 2011 – Nov 23, 2026ActiveRegistration details
- Analysis ID
- 69abf7c654a5cd724117f1b9e1ab069e
- Customs Code
- DHA00602293001
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
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.1220 電極記錄導管或電極記錄探頭
- Import Information
- import
Dates and status
- Registration Date
- Nov 23, 2011
- Expiry Date
- Nov 23, 2026
About this record
Access comprehensive regulatory information for "Japan Lai Fuen" Fix fixed bent electrode catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 69abf7c654a5cd724117f1b9e1ab069e and manufactured by JAPAN LIFELINE CO., LTD.;; Japan Lifeline Co., Ltd. Toda Factory. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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