Taiwan FDA registration e54acb13d87a5e9d54ddc38ecbf1fd76
"Asahi" Restrix hollow dialyzer
TW: “旭”瑞斯特利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
- e54acb13d87a5e9d54ddc38ecbf1fd76
- Customs Code
- DHA00602336909
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" Restrix 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 e54acb13d87a5e9d54ddc38ecbf1fd76 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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