Taiwan FDA registration 59d3ada1b3b2b1c9fd7d3c9d544f060d

"Remon" thyroid microsomal antigen autologous antibody detection kit

TW: "銳盟" 甲狀腺微粒體抗原自體抗體檢測套組

Taiwan·Risk Class 2·REMEL EUROPE LIMITED·Registered Feb 21, 2006 – Feb 21, 2026Expired

Registration details

Analysis ID: 59d3ada1b3b2b1c9fd7d3c9d544f060d
Customs Code: DHA00601603301

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 thyroid microsomal antigen.
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 "Remon" thyroid microsomal antigen autologous antibody detection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 59d3ada1b3b2b1c9fd7d3c9d544f060d and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..

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