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SD BIOSENSOR STANDARD F RSV Ag FIA (Non-Sterile) - Taiwan Registration 5a0631a110e20fba3b664c6da7b034b0

Access comprehensive regulatory information for SD BIOSENSOR STANDARD F RSV 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 5a0631a110e20fba3b664c6da7b034b0 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.

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5a0631a110e20fba3b664c6da7b034b0
Registration Details
Taiwan FDA Registration: 5a0631a110e20fba3b664c6da7b034b0
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Device Details

SD BIOSENSOR STANDARD F RSV Ag FIA (Non-Sterile)
TW: โ€œ้€Ÿๅพ—็™พๆฃฎโ€ ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

5a0631a110e20fba3b664c6da7b034b0

Ministry of Health Medical Device Import No. 020047

DHA09402004701

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Respiratory Fusion Cell Virus Serological Reagent (C.3480)".

C Immunology and microbiology devices

C3480 Respiratory Fusion Cell Virus Serological Reagent

Imported from abroad

Dates and Status

Jan 21, 2019

Jan 21, 2024