Taiwan FDA registration d73848b2a1b85c5542f4d331e40e9b17
"Japan Lai Fuen" Ipita unidirectional electrode catheter
TW: “日本來富恩”意皮斯塔單向電極導管
Taiwan·Risk Class 2·JAPAN LIFELINE CO., LTD.;; Japan Lifeline Co., Ltd. Toda Factory·Registered Oct 03, 2011 – Oct 03, 2026ActiveRegistration details
- Analysis ID
- d73848b2a1b85c5542f4d331e40e9b17
- Customs Code
- DHA00602283201
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
- Oct 03, 2011
- Expiry Date
- Oct 03, 2026
About this record
Access comprehensive regulatory information for "Japan Lai Fuen" Ipita unidirectional 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 d73848b2a1b85c5542f4d331e40e9b17 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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