Taiwan FDA registration 55bc289b4541d9c161a7b9da85edb2a4
"Sharp" thyroglobulin autologous antibody test kit
TW: "銳盟" 甲狀腺球蛋白自體抗體檢測套組
Taiwan·Risk Class 2·REMEL EUROPE LIMITED·Registered Feb 21, 2006 – Feb 21, 2026ExpiredRegistration details
- Analysis ID
- 55bc289b4541d9c161a7b9da85edb2a4
- Customs Code
- DHA00601603209
Company information
- Manufacturer
- REMEL EUROPE LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- THERMO FISHER SCIENTIFIC TAIWAN CO., LTD.
Product details
- Intended Use
- Semi-quantitative detection of autoantibodies to human thyroglobulin.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5870 甲狀腺自體抗體免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Feb 21, 2006
- Expiry Date
- Feb 21, 2026
About this record
Access comprehensive regulatory information for "Sharp" thyroglobulin autologous antibody test kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55bc289b4541d9c161a7b9da85edb2a4 and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC 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