Pure Global

Kaiwu Influenza Type A and B Kits - Taiwan Registration 52cbddc1649f5bb3da505d76beece3e5

Access comprehensive regulatory information for Kaiwu Influenza Type A and B Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 52cbddc1649f5bb3da505d76beece3e5 and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Tainan Branch.

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
52cbddc1649f5bb3da505d76beece3e5
Registration Details
Taiwan FDA Registration: 52cbddc1649f5bb3da505d76beece3e5
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Kaiwu Influenza Type A and B Kits
TW: ้–‹็‰ฉ็ง‘ๆŠ€ๆต่กŒๆ€งๆ„Ÿๅ†’Aๅž‹ๅŠBๅž‹่ฉฆๅŠ‘็›’
Risk Class 1
Cancelled

Registration Details

52cbddc1649f5bb3da505d76beece3e5

DHA04400653803

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".

C Immunology and microbiology

C.3330 ๆตๆ„Ÿ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Feb 25, 2008

Feb 25, 2013

Jun 11, 2015

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ