Taiwan FDA registration 9ee5080bcf7a19384f2a541213979b4e
Asahi Kasei Rest's hemodialyzer
TW: 旭化成瑞斯特血液透析器
Taiwan·Risk Class 2·Kawasumi Laboratories (Thailand) Co., Ltd.(Korat)·Registered Oct 19, 2011 – Oct 19, 2016CancelledRegistration details
- Analysis ID
- 9ee5080bcf7a19384f2a541213979b4e
- Customs Code
- DHA00602295606
Company information
- Manufacturer Country
- Thailand
- 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
- Oct 19, 2011
- Expiry Date
- Oct 19, 2016
- Cancellation Date
- Jan 28, 2016
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for Asahi Kasei Rest's hemodialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ee5080bcf7a19384f2a541213979b4e and manufactured by Kawasumi Laboratories (Thailand) Co., Ltd.(Korat). The authorized representative in Taiwan is Taiwan Asahi Kasei Medical Device Trading Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices