Taiwan FDA registration 55f7fec6ded4ab45bfbd2b128828d1e4
SEBIA CDT MINICAP CALIBRATORS
TW: 賽比亞 迷你型毛細管缺醣攜鐵蛋白檢測校正液
Taiwan·Risk Class 2·MD·SEBIA·Registered Jun 13, 2022 – Jun 13, 2027ActiveRegistration details
- Analysis ID
- 55f7fec6ded4ab45bfbd2b128828d1e4
- License Form
- Ministry of Health Medical Device Import No. 035666
- Customs Code
- DHA05603566601
Company information
- Manufacturer
- SEBIA
- Manufacturer Country
- France
- Authorized Representative
- SCN TRADING COMPANY LIMITED
Product details
- Intended Use
- This product is used with the SEBIA capillary electrophoresis system for the calibration of the CDT-IFCC fragment (disialidylated ferritin) quantification method.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1150 calibrate
- Import Information
- Imported from abroad; GMP
Dates and status
- Registration Date
- Jun 13, 2022
- Expiry Date
- Jun 13, 2027
About this record
Access comprehensive regulatory information for SEBIA CDT MINICAP CALIBRATORS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55f7fec6ded4ab45bfbd2b128828d1e4 and manufactured by SEBIA. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.
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