Taiwan FDA registration 4af722bd592af6754c9442001a75d3a2
"Medical technology" dialysis device for personal use
TW: “醫技”個人用透析裝置
Taiwan·Risk Class 2·MED-TECH INC. SAITAMA FACTORY·Registered Jan 29, 2010 – Jan 29, 2015CancelledRegistration details
- Analysis ID
- 4af722bd592af6754c9442001a75d3a2
- Customs Code
- DHA00602056609
Company information
- Manufacturer
- MED-TECH INC. SAITAMA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- Taiwan Asahi Kasei Medical Device Trading 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.5820 血液透析系統及其附件
- Import Information
- import
Dates and status
- Registration Date
- Jan 29, 2010
- Expiry Date
- Jan 29, 2015
- Cancellation Date
- Jan 28, 2016
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Medical technology" dialysis device for personal use in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4af722bd592af6754c9442001a75d3a2 and manufactured by MED-TECH INC. SAITAMA FACTORY. The authorized representative in Taiwan is Taiwan Asahi Kasei Medical Device Trading Co., Ltd.
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