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Ameri Chlamydomydomiae Test Set (Unsterilized) - Taiwan Registration 8ef831f919f10d25981fe1167fdb0bd7

Access comprehensive regulatory information for Ameri Chlamydomydomiae 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 8ef831f919f10d25981fe1167fdb0bd7 and manufactured by AMERITEK USA. 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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8ef831f919f10d25981fe1167fdb0bd7
Registration Details
Taiwan FDA Registration: 8ef831f919f10d25981fe1167fdb0bd7
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Device Details

Ameri Chlamydomydomiae Test Set (Unsterilized)
TW: ไบž็พŽๅˆฉๅฏๆŠซ่กฃ่Œๆชข้ฉ—่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

8ef831f919f10d25981fe1167fdb0bd7

DHA04600100103

Company Information

China

Product Details

Limited to the first grade identification range of Chlamydomydia serological reagent (C.3120) for the management of medical devices.

C Immunology and microbiology

C.3120 ๆŠซ่กฃ่Œ่ก€ๆธ…่ฉฆๅŠ‘

Chinese goods;; input

Dates and Status

Aug 02, 2010

Aug 02, 2020

Jun 22, 2022

Cancellation Information

Logged out

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