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Badiek Rotavirus/Adenovirus Test Reagent - Tube Solution - Taiwan Registration ec56c3abaea4a5393162f460c41fb260

Access comprehensive regulatory information for Badiek Rotavirus/Adenovirus Test Reagent - Tube Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec56c3abaea4a5393162f460c41fb260 and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is MEDRICH INSTRUMENT 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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ec56c3abaea4a5393162f460c41fb260
Registration Details
Taiwan FDA Registration: ec56c3abaea4a5393162f460c41fb260
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Device Details

Badiek Rotavirus/Adenovirus Test Reagent - Tube Solution
TW: ๅทด่ฟช้ตๅ…‹่ผช็‹€็—…ๆฏ’/่…บ็—…ๆฏ’ๆชข้ฉ—่ฉฆๅŠ‘-ๅ“็ฎกๆถฒ
Risk Class 2

Registration Details

ec56c3abaea4a5393162f460c41fb260

DHA05603587701

Company Information

Korea, Republic of

Product Details

This product is used for quality management of rotavirus/adenovirus testing reagents manufactured by Boditech Med Inc. for in vitro diagnostic purposes.

A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical)

Input;; QMS/QSD

Dates and Status

Nov 02, 2022

Nov 02, 2027