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SD BIOSENSOR STANDARD F Legionella Ag FIA (Non-Sterile) - Taiwan Registration acf3f196b38ebb9c9c35e322be6426c2

Access comprehensive regulatory information for SD BIOSENSOR STANDARD F Legionella 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 acf3f196b38ebb9c9c35e322be6426c2 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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acf3f196b38ebb9c9c35e322be6426c2
Registration Details
Taiwan FDA Registration: acf3f196b38ebb9c9c35e322be6426c2
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Device Details

SD BIOSENSOR STANDARD F Legionella Ag FIA (Non-Sterile)
TW: โ€œ้€Ÿๅพ—็™พๆฃฎโ€้€€ไผ่ปไบบ็—‡่žขๅ…‰้…ต็ด ๅ…็–ซๅˆ†ๆžๆชขๆธฌๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

acf3f196b38ebb9c9c35e322be6426c2

Ministry of Health Medical Device Import No. 020030

DHA09402003007

Company Information

Korea, Republic of

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

Jan 16, 2019

Jan 16, 2024