Taiwan FDA registration e306884c4167921c4d01ee125de94aac
Sismer urine analyzer tube solution (unsterilized)
TW: 西斯美尿液分析儀品管液(未滅菌)
Registration details
- Analysis ID
- e306884c4167921c4d01ee125de94aac
- Customs Code
- DHA04400225905
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- Sandong Instrument Co., Ltd
Product details
- Intended Use
- This quality control solution is used to monitor the quality management of the fully automated urine cell analyzer (Sysmex UF series device).
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- import
Dates and status
- Registration Date
- Dec 14, 2005
- Expiry Date
- Dec 14, 2015
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Sismer urine analyzer tube solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e306884c4167921c4d01ee125de94aac and manufactured by SYSMEX CORPORATION;; SYSMEX INTERNATIONAL REAGENTS CO., LTD., ONO FACTORY. The authorized representative in Taiwan is Sandong Instrument 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