Taiwan FDA registration 03404621a56812b4ce2c049a6e3326de
"Asahi" Rest Aix hollow dialyzer
TW: “旭”瑞斯特艾克斯中空系型透析器
Taiwan·Risk Class 2·Asahi Kasei Medical Co.,Ltd.Okatomi Plant·Registered Mar 08, 2012 – Mar 08, 2017CancelledRegistration details
- Analysis ID
- 03404621a56812b4ce2c049a6e3326de
- Customs Code
- DHA00602337007
Company information
- Manufacturer
- Asahi Kasei Medical Co.,Ltd.Okatomi Plant
- 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
- Mar 08, 2012
- Expiry Date
- Mar 08, 2017
- Cancellation Date
- Jan 28, 2016
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Asahi" Rest Aix hollow dialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03404621a56812b4ce2c049a6e3326de and manufactured by Asahi Kasei Medical Co.,Ltd.Okatomi Plant. The authorized representative in Taiwan is Taiwan Asahi Kasei Medical Device Trading Co., Ltd.
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