Taiwan FDA registration f5e8c662b680c987c57cb8a62477fe86
"Medical technology" blood purification device
TW: "醫技" 血液淨化裝置
Taiwan·Risk Class 2·MED-TECH INC. SAITAMA FACTORY·Registered Jan 03, 2005 – Jan 03, 2020CancelledRegistration details
- Analysis ID
- f5e8c662b680c987c57cb8a62477fe86
- Customs Code
- DHA00601098701
Company information
- Manufacturer
- MED-TECH INC. SAITAMA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- EXCELSIOR MEDICAL CO., LTD.
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.5860 高滲透性之血液透析系統
- Import Information
- import
Dates and status
- Registration Date
- Jan 03, 2005
- Expiry Date
- Jan 03, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medical technology" blood purification device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5e8c662b680c987c57cb8a62477fe86 and manufactured by MED-TECH INC. SAITAMA FACTORY. The authorized representative in Taiwan is EXCELSIOR MEDICAL CO., LTD..
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