Taiwan FDA registration 5aba8298360c8cef8c7eaf7fb49891d1
“Japan Lifeline” BeeAT Atrial Cardioversion Catheter
TW: “日本來富恩” 心腔內除顫導管
Taiwan·Risk Class 3·MD·Japan Lifeline Co., Ltd. Toda Factory·Registered May 28, 2014 – May 28, 2024ExpiredRegistration details
- Analysis ID
- 5aba8298360c8cef8c7eaf7fb49891d1
- License Form
- Ministry of Health Medical Device Import No. 025948
- Customs Code
- DHA05602594802
Company information
- Manufacturer
- Japan Lifeline Co., Ltd. Toda Factory
- 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 devices
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 28, 2014
- Expiry Date
- May 28, 2024
About this record
Access comprehensive regulatory information for “Japan Lifeline” BeeAT Atrial Cardioversion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5aba8298360c8cef8c7eaf7fb49891d1 and manufactured by Japan Lifeline Co., Ltd. Toda Factory. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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