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"Bioken" Shigella antiserum reagent (unsterilized) - Taiwan Registration dc67325079b38a63583e8fdc13e9c323

Access comprehensive regulatory information for "Bioken" Shigella antiserum 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 dc67325079b38a63583e8fdc13e9c323 and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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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dc67325079b38a63583e8fdc13e9c323
Registration Details
Taiwan FDA Registration: dc67325079b38a63583e8fdc13e9c323
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Device Details

"Bioken" Shigella antiserum reagent (unsterilized)
TW: "็”Ÿ็ ”" ๅฟ—่ณ€ๆฐ่ŒๆŠ—่ก€ๆธ…่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

dc67325079b38a63583e8fdc13e9c323

DHA04400898308

Company Information

Japan

Product Details

It is limited to the first-level identification scope of Shigella serum reagent (C.3660) in the classification and grading management measures for medical devices.

C Immunology and microbiology

C.3660 ๅฟ—่ณ€ๆฐๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Jul 12, 2010

Jul 12, 2025