Taiwan FDA registration b825c3a41e8ff37b7166a4ecbd1192da
“Fukuda Denshi” VaSera Sphygmomanometer and Sphygmograph
TW: “福田電子”血壓脈波計
Taiwan·Risk Class 2·MD·FUKUDA DENSHI CO. LTD. SHIROI FACTORY·Registered Aug 17, 2018 – Aug 17, 2028ActiveRegistration details
- Analysis ID
- b825c3a41e8ff37b7166a4ecbd1192da
- License Form
- Ministry of Health Medical Device Import No. 031502
- Customs Code
- DHA05603150200
Company information
- Manufacturer
- FUKUDA DENSHI CO. LTD. SHIROI FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- SOAR INSTRUMENT-TECH. CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1130 Non-invasive blood pressure measurement system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 17, 2018
- Expiry Date
- Aug 17, 2028
About this record
Access comprehensive regulatory information for “Fukuda Denshi” VaSera Sphygmomanometer and Sphygmograph in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b825c3a41e8ff37b7166a4ecbd1192da and manufactured by FUKUDA DENSHI CO. LTD. SHIROI FACTORY. The authorized representative in Taiwan is SOAR INSTRUMENT-TECH. CO., LTD..
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