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"Puse" Chlamydia Enzyme Immunoassay Assay Kit (Unsterilized) - Taiwan Registration fa00668317d80e3c40da2448dcff7949

Access comprehensive regulatory information for "Puse" Chlamydia Enzyme Immunoassay Assay Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fa00668317d80e3c40da2448dcff7949 and manufactured by GENERAL BIOLOGICALS CORP.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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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fa00668317d80e3c40da2448dcff7949
Registration Details
Taiwan FDA Registration: fa00668317d80e3c40da2448dcff7949
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Device Details

"Puse" Chlamydia Enzyme Immunoassay Assay Kit (Unsterilized)
TW: "ๆ™ฎ็”Ÿ" ๆŠซ่กฃ่Œ้…ต็ด ๅ…็–ซๆชข้ฉ—ๅˆ†ๆžๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

fa00668317d80e3c40da2448dcff7949

Company Information

Taiwan, Province of China

Product Details

It is limited to the first-level identification scope of Chlamydia serum reagent (C.3120) in the classification and grading management measures for medical devices.

C Immunology and microbiology

C.3120 ๆŠซ่กฃ่Œ่ก€ๆธ…่ฉฆๅŠ‘

Domestic

Dates and Status

Jun 04, 2014

Jun 04, 2024