Pure Global

Kaiwo Technology Influenza A and B Kits - Taiwan Registration 139f1f31453f9cc1a7e26b612be2294b

Access comprehensive regulatory information for Kaiwo Technology Influenza 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 139f1f31453f9cc1a7e26b612be2294b and manufactured by HANGZHOU GENESIS BIODETECTION AND BIOCONTROL CO., LTD;; EQUAL ACCESS TO SCIENTIFIC EXCELLENCE. 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
139f1f31453f9cc1a7e26b612be2294b
Registration Details
Taiwan FDA Registration: 139f1f31453f9cc1a7e26b612be2294b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Kaiwo Technology Influenza A and B Kits
TW: ้–‹็‰ฉ็ง‘ๆŠ€ๆตๆ„ŸAๅž‹ๅŠBๅž‹่ฉฆๅŠ‘็›’
Risk Class 1
Cancelled

Registration Details

139f1f31453f9cc1a7e26b612be2294b

DHA04600078802

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‘

Contract manufacturing;; Input;; Chinese goods

Dates and Status

Sep 08, 2009

Sep 08, 2014

Jun 25, 2018

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ