Taiwan FDA registration 295cbb0c68f695e40826517b092fde5d
"Sanyo Electronics" plasmapheresis filter
TW: “山陽電子”血漿置換過濾機
Taiwan·Risk Class 2·SANYO ELECTRONIC INDUSTRIES CO., LTD.·Registered Feb 17, 2011 – Feb 17, 2026ExpiredRegistration details
- Analysis ID
- 295cbb0c68f695e40826517b092fde5d
- Customs Code
- DHA00602216300
Company information
- Manufacturer
- SANYO ELECTRONIC INDUSTRIES CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- K2 INTERNATIONAL MEDICAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5665 透析用水之淨化系統
- Import Information
- import
Dates and status
- Registration Date
- Feb 17, 2011
- Expiry Date
- Feb 17, 2026
About this record
Access comprehensive regulatory information for "Sanyo Electronics" plasmapheresis filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 295cbb0c68f695e40826517b092fde5d and manufactured by SANYO ELECTRONIC INDUSTRIES CO., LTD.. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..
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