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"Likuan" Legionnaires' Pneumonia Antigen Urine Test Reagent (Unsterilized) - Taiwan Registration 5fc998b04713805797f65cdee45ea1bf

Access comprehensive regulatory information for "Likuan" Legionnaires' Pneumonia Antigen Urine 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 5fc998b04713805797f65cdee45ea1bf and manufactured by AMERITEK. The authorized representative in Taiwan is LIKWANG INSTRUMENTS 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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5fc998b04713805797f65cdee45ea1bf
Registration Details
Taiwan FDA Registration: 5fc998b04713805797f65cdee45ea1bf
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Device Details

"Likuan" Legionnaires' Pneumonia Antigen Urine Test Reagent (Unsterilized)
TW: "็ซ‹ๅฏฌ" ้€€ไผ่ปไบบ็—‡่‚บ็‚ŽๆŠ—ๅŽŸๅฐฟๆถฒๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

5fc998b04713805797f65cdee45ea1bf

DHA09600219106

Company Information

China

Product Details

Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.

C Immunology and microbiology

C.3300 ๅ—œ่ก€ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

Input;; Chinese goods

Dates and Status

Aug 08, 2014

Aug 08, 2019

Jun 22, 2022

Cancellation Information

Logged out

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