Taiwan FDA registration 3c67d06f3e14cb7c7d3c21733b37a521

"SYSMEX" Quality control material (assayed and unassayed) (Non-Sterile)

TW: "希森美康" 品管材料(分析與非分析) (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·LINE·Registered Nov 13, 2018 – Nov 13, 2028Active
Registration details
Analysis ID
3c67d06f3e14cb7c7d3c21733b37a521
License Form
Ministry of Health Medical Device Import No. 019816
Customs Code
DHA09401981606
Company information
Manufacturer
LINE
Manufacturer Country
United States
Authorized Representative
SYSMEX TAIWAN CO., LTD.
Product details
Intended Use
Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A1660 Quality Control Materials (Analytical and Non-Analytical)
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 13, 2018
Expiry Date
Nov 13, 2028
About this record

Access comprehensive regulatory information for "SYSMEX" Quality control material (assayed and unassayed) (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3c67d06f3e14cb7c7d3c21733b37a521 and manufactured by LINE. The authorized representative in Taiwan is SYSMEX TAIWAN 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