Pure Global

"Thermo Fisher Scientific" Legionella Test (Non-Sterile) - Taiwan Registration c81b402e89efeb5672e9111a2d72d817

Access comprehensive regulatory information for "Thermo Fisher Scientific" Legionella Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c81b402e89efeb5672e9111a2d72d817 and manufactured by REMEL INC.. 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
c81b402e89efeb5672e9111a2d72d817
Registration Details
Taiwan FDA Registration: c81b402e89efeb5672e9111a2d72d817
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Thermo Fisher Scientific" Legionella Test (Non-Sterile)
TW: "่ณฝ้ป˜้ฃ›ไธ–็ˆพ็ง‘ๆŠ€" ้€€ไผ่ปไบบ่‚บ็‚ŽๅฐฟๆถฒๆŠ—ๅŽŸๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c81b402e89efeb5672e9111a2d72d817

Ministry of Health Medical Device Import No. 017178

DHA09401717803

Company Information

United States

Product Details

Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.

C Immunology and microbiology devices

C3300 Haemophilus serology

Imported from abroad

Dates and Status

Nov 16, 2016

Nov 16, 2021