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"STIK" Influenza A/B Rapid Test Set (Unsterilized) - Taiwan Registration 7f2f995128566ad943615e4fb26befd3

Access comprehensive regulatory information for "STIK" Influenza A/B Rapid 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 7f2f995128566ad943615e4fb26befd3 and manufactured by CTK BIOTECH, INC.. 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.

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7f2f995128566ad943615e4fb26befd3
Registration Details
Taiwan FDA Registration: 7f2f995128566ad943615e4fb26befd3
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Device Details

"STIK" Influenza A/B Rapid Test Set (Unsterilized)
TW: "ๆ–ฏ่ฟชๅ…‹" ๆตๆ„ŸA/Bๅž‹ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

7f2f995128566ad943615e4fb26befd3

DHA04401126300

Company Information

United States

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‘

import

Dates and Status

Jan 03, 2012

Jan 03, 2017

Nov 17, 2019

Cancellation Information

Logged out

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