Pure Global

“SD BIOSENSOR” STANDARD F Adeno Respi Ag FIA (Non-Sterile) - Taiwan Registration 4bc7522e159385af173767681d1b6f98

Access comprehensive regulatory information for “SD BIOSENSOR” STANDARD F Adeno Respi Ag FIA (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 4bc7522e159385af173767681d1b6f98 and manufactured by SD BIOSENSOR, Inc.. The authorized representative in Taiwan is CREATIVE LIFE SCIENCE 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
4bc7522e159385af173767681d1b6f98
Registration Details
Taiwan FDA Registration: 4bc7522e159385af173767681d1b6f98
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“SD BIOSENSOR” STANDARD F Adeno Respi Ag FIA (Non-Sterile)
TW: “速得百森” 腺病毒(呼吸道)檢驗試劑(未滅菌)
Risk Class 1
MD

Registration Details

4bc7522e159385af173767681d1b6f98

Ministry of Health Medical Device Import No. 022380

DHA09402238005

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".

C Immunology and microbiology devices

C3020 adenovirus serum reagent

Imported from abroad

Dates and Status

Mar 11, 2021

Mar 11, 2026