Pure Global

"Avi" Rotavirus/Adenovirus Rapid Test Reagent (Unsterilized) - Taiwan Registration 896e0397ca36abfd58acc6196e37986e

Access comprehensive regulatory information for "Avi" Rotavirus/Adenovirus 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 896e0397ca36abfd58acc6196e37986e and manufactured by AVE SCIENCE & TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is DiaTech Technology 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
896e0397ca36abfd58acc6196e37986e
Registration Details
Taiwan FDA Registration: 896e0397ca36abfd58acc6196e37986e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Avi" Rotavirus/Adenovirus Rapid Test Reagent (Unsterilized)
TW: โ€œๆ„›ๅจโ€ ่ผช็‹€็—…ๆฏ’/่…บ็—…ๆฏ’ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

896e0397ca36abfd58acc6196e37986e

DHA09600428601

Company Information

Product Details

It is limited to the first-level identification scope of the "Adenovirus Serum Reagent (C.3020)" and "Poliovirus Serum Reagent (C.3405)" of the Classification and Grading Management Measures for Medical Devices.

C Immunology and microbiology

C.3020 ่…บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘;; C.3405 ๅฐๅ…’้บป็—บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Chinese goods;; input

Dates and Status

Aug 13, 2020

Aug 13, 2025