Pure Global

"MIZUHO" Adenovirus test kit (Non-sterile) - Taiwan Registration 163b5661f32c0c186915aeab60e0e200

Access comprehensive regulatory information for "MIZUHO" Adenovirus test kit (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 163b5661f32c0c186915aeab60e0e200 and manufactured by MIZUHO MEDY CO., LTD.. The authorized representative in Taiwan is LINKSEAS TRADING 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
163b5661f32c0c186915aeab60e0e200
Registration Details
Taiwan FDA Registration: 163b5661f32c0c186915aeab60e0e200
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"MIZUHO" Adenovirus test kit (Non-sterile)
TW: "็พŽๆ—ฅๅ’Œ"่…บ็—…ๆฏ’ๆชข้ฉ—่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

163b5661f32c0c186915aeab60e0e200

Ministry of Health Medical Device Import No. 018791

DHA09401879101

Company Information

Japan

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".

C Immunology and microbiology devices

C3020 adenovirus serum reagent

Imported from abroad

Dates and Status

Feb 05, 2018

Feb 05, 2023