Taiwan FDA registration f3b68dd7ee50ea33869ea3e9560e153c
"Japan Lai Fuen" Ambisch catheter guide
TW: “日本來富恩”安必施導管導引器
Taiwan·Risk Class 2·JAPAN LIFELINE CO., LTD.;; Japan Lifeline Co., Ltd. Toda Factory·Registered Nov 21, 2016 – Nov 21, 2026ActiveRegistration details
- Analysis ID
- f3b68dd7ee50ea33869ea3e9560e153c
- Customs Code
- DHA05602911402
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.1340 Catheter Introducers
- Import Information
- import
Dates and status
- Registration Date
- Nov 21, 2016
- Expiry Date
- Nov 21, 2026
About this record
Access comprehensive regulatory information for "Japan Lai Fuen" Ambisch catheter guide in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3b68dd7ee50ea33869ea3e9560e153c 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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