Taiwan FDA registration d60ad32dd48ce6d3bb2e76b7fe76188a
"Japan Lai Fuen" Sneak bidirectional electrode catheter
TW: “日本來富恩”史奈克雙向電極導管
Taiwan·Risk Class 2·JAPAN LIFELINE CO., LTD.;; Japan Lifeline Co., Ltd. Toda Factory·Registered Dec 01, 2011 – Dec 01, 2026ActiveRegistration details
- Analysis ID
- d60ad32dd48ce6d3bb2e76b7fe76188a
- Customs Code
- DHA00602294603
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
- Dec 01, 2011
- Expiry Date
- Dec 01, 2026
About this record
Access comprehensive regulatory information for "Japan Lai Fuen" Sneak bidirectional 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 d60ad32dd48ce6d3bb2e76b7fe76188a 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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