Taiwan FDA registration aff3e868e06220927be4ea0854719ec6
Sisme urine quality solution (unsterilized)
TW: 西斯美尿液品管液 (未滅菌)
Registration details
- Analysis ID
- aff3e868e06220927be4ea0854719ec6
- Customs Code
- DHA04400006001
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- Sandong Instrument Co., Ltd
Product details
- Intended Use
- It is used for quality control of fully automated urine cell analyzers.
- 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
- May 18, 2005
- Expiry Date
- May 18, 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 urine quality 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 aff3e868e06220927be4ea0854719ec6 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