Taiwan FDA registration 5a2c505585b75c9d613e121e3e0517d2
Solidile plasma separator
TW: 固拉力血漿分離器
Taiwan·Risk Class 2·ASAHI KASEI KURARAY MEDICIAL CO., LTD. OITA WORKS·Registered Jul 04, 2008 – Jul 04, 2013CancelledRegistration details
- Analysis ID
- 5a2c505585b75c9d613e121e3e0517d2
- Customs Code
- DHA00601909101
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MUTUAL 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
- Jul 04, 2008
- Expiry Date
- Jul 04, 2013
- Cancellation Date
- Sep 26, 2016
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Solidile plasma separator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5a2c505585b75c9d613e121e3e0517d2 and manufactured by ASAHI KASEI KURARAY MEDICIAL CO., LTD. OITA WORKS. The authorized representative in Taiwan is MUTUAL TRADING CO., LTD..
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