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"Sekisui" Bacterial Vaginosis Test (Non-Sterile) - Taiwan Registration d2c1620c43a04b76a617bbe278586d39

Access comprehensive regulatory information for "Sekisui" Bacterial Vaginosis Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d2c1620c43a04b76a617bbe278586d39 and manufactured by GRYPHUS DIAGNOSTICS, LLC. The authorized representative in Taiwan is ARSENALS IVD CO., LTD..

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d2c1620c43a04b76a617bbe278586d39
Registration Details
Taiwan FDA Registration: d2c1620c43a04b76a617bbe278586d39
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Device Details

"Sekisui" Bacterial Vaginosis Test (Non-Sterile)
TW: "็ธพ็ฉ—" ็ดฐ่Œๆ€ง้™ฐ้“็‚Žๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d2c1620c43a04b76a617bbe278586d39

Ministry of Health Medical Device Import No. 017559

DHA09401755902

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".

C Immunology and microbiology devices

C2660 Microbial identification and assay equipment

Imported from abroad

Dates and Status

Mar 06, 2017

Mar 06, 2022