Taiwan FDA registration d04e08a49644d22a3a7bfe5d7bf2dcc4
“Fukuda Sangyo” SpiroAnalyzer
TW: “福田”肺功能機
Taiwan·Risk Class 2·MD·FUKUDA SANGYO CO., LTD. Takata factory·Registered May 27, 2020 – May 27, 2025ExpiredRegistration details
- Analysis ID
- d04e08a49644d22a3a7bfe5d7bf2dcc4
- License Form
- Ministry of Health Medical Device Import No. 033603
- Customs Code
- DHA05603360303
Company information
- Manufacturer
- FUKUDA SANGYO CO., LTD. Takata factory
- Manufacturer Country
- Japan
- Authorized Representative
- IN GOAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D1840 Spirometer for diagnosis
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 27, 2020
- Expiry Date
- May 27, 2025
About this record
Access comprehensive regulatory information for “Fukuda Sangyo” SpiroAnalyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d04e08a49644d22a3a7bfe5d7bf2dcc4 and manufactured by FUKUDA SANGYO CO., LTD. Takata factory. The authorized representative in Taiwan is IN GOAL CO., LTD..
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