Taiwan FDA registration 34ce648220e64dfd88818d7086655d38
Sisme reticulated red blood cell diversion
TW: 西斯美網狀紅血球導流液
Taiwan·Risk Class 1·SYSMEX CORPORATION;; SYSMEX INTERNATIONAL REAGENTS CO., LTD., ONO FACTORY·Registered May 26, 2005 – May 26, 2015CancelledRegistration details
- Analysis ID
- 34ce648220e64dfd88818d7086655d38
- Customs Code
- DHA04400010609
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- Sandong Instrument Co., Ltd
Product details
- Intended Use
- A solution used in the SYSMEX Automated Mesh Red Blood Cell Analyzer that forms a cylindrical flow of diversion around the diluted sample.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.4010 Reaction Reagents for General Purposes
- Import Information
- import
Dates and status
- Registration Date
- May 26, 2005
- Expiry Date
- May 26, 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 Sisme reticulated red blood cell diversion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 34ce648220e64dfd88818d7086655d38 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