Pure Global

"Remon" thyroid microsomal antigen autologous antibody detection kit - Taiwan Registration 59d3ada1b3b2b1c9fd7d3c9d544f060d

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..

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 Database
Powered by Pure Global AI
89,000+ Devices
59d3ada1b3b2b1c9fd7d3c9d544f060d
Registration Details
Taiwan FDA Registration: 59d3ada1b3b2b1c9fd7d3c9d544f060d
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Remon" thyroid microsomal antigen autologous antibody detection kit
TW: "้Šณ็›Ÿ" ็”ฒ็‹€่…บๅพฎ็ฒ’้ซ”ๆŠ—ๅŽŸ่‡ช้ซ”ๆŠ—้ซ”ๆชขๆธฌๅฅ—็ต„
Risk Class 2

Registration Details

59d3ada1b3b2b1c9fd7d3c9d544f060d

DHA00601603301

Company Information

United Kingdom

Product Details

Semi-quantitative detection of autoantibodies to human thyroid microsomal antigen.

C Immunology and microbiology

C.5870 ็”ฒ็‹€่…บ่‡ช้ซ”ๆŠ—้ซ”ๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Feb 21, 2006

Feb 21, 2026