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"Torch" adenovirus test set (unsterilized) - Taiwan Registration 6c7e1ee3f1fa019a0edb4101fc234014

Access comprehensive regulatory information for "Torch" adenovirus test set (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6c7e1ee3f1fa019a0edb4101fc234014 and manufactured by HANGZHOU GENESIS BIODETECTION AND BIOCONTROL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY 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.

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6c7e1ee3f1fa019a0edb4101fc234014
Registration Details
Taiwan FDA Registration: 6c7e1ee3f1fa019a0edb4101fc234014
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Device Details

"Torch" adenovirus test set (unsterilized)
TW: "็‚ฌๅˆ" ่…บ็—…ๆฏ’ๆชข้ฉ—่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

6c7e1ee3f1fa019a0edb4101fc234014

DHA09600198104

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

C.3020 ่…บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Input;; Chinese goods

Dates and Status

Sep 11, 2013

Sep 11, 2018

May 19, 2022

Cancellation Information

Logged out

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