Taiwan FDA registration e699586bea1e7b9a05a57abf0dd7f995

Xinkehua rapid thyroid-stimulating receptor autologous antibody enzyme analysis reagent

TW: 新科化快速促甲狀腺接受器自體抗體酵素分析試劑

Taiwan·Risk Class 2·RSR LIMITED·Registered Aug 05, 2010 – Aug 05, 2025Expired

Registration details

Analysis ID: e699586bea1e7b9a05a57abf0dd7f995
Customs Code: DHA00602139207

Company information

Manufacturer: RSR LIMITED
Manufacturer Country: United Kingdom
Authorized Representative: NEW SCIENTIFIC EQUIPMENT CO., LTD.

Product details

Intended Use: In vitro diagnostic use, using enzyme immunoassay to quantify thyroid-stimulating receptor autoantibodies in serum.
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: Aug 05, 2010
Expiry Date: Aug 05, 2025

About this record

Access comprehensive regulatory information for Xinkehua rapid thyroid-stimulating receptor autologous antibody enzyme analysis reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e699586bea1e7b9a05a57abf0dd7f995 and manufactured by RSR LIMITED. The authorized representative in Taiwan is NEW SCIENTIFIC EQUIPMENT 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.