Pure Global

"Wonderfu" Influenza A/B Virus Rapid Test Reagent (Unsterilized) - Taiwan Registration 0d2cf3c819b4d25aead388d034b91b10

Access comprehensive regulatory information for "Wonderfu" Influenza A/B Virus Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0d2cf3c819b4d25aead388d034b91b10 and manufactured by WONDFO BIOTECH CO., LTD. The authorized representative in Taiwan is LIKWANG INSTRUMENTS 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
0d2cf3c819b4d25aead388d034b91b10
Registration Details
Taiwan FDA Registration: 0d2cf3c819b4d25aead388d034b91b10
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Wonderfu" Influenza A/B Virus Rapid Test Reagent (Unsterilized)
TW: "่ฌๅพทๅญš" A/Bๅž‹ๆตๆ„Ÿ็—…ๆฏ’ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0d2cf3c819b4d25aead388d034b91b10

DHA09600264506

Company Information

China

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‘

Chinese goods;; input

Dates and Status

Feb 25, 2016

Feb 25, 2021

Oct 12, 2023

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€