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"Thermo Fisher Scientific" Rotavirus Antigen Rapid Test (Non-sterile) - Taiwan Registration 8fe0e19c3e46cc11aa8c0a4c00446c97

Access comprehensive regulatory information for "Thermo Fisher Scientific" Rotavirus Antigen Rapid 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 8fe0e19c3e46cc11aa8c0a4c00446c97 and manufactured by REMEL INC.. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN 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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8fe0e19c3e46cc11aa8c0a4c00446c97
Registration Details
Taiwan FDA Registration: 8fe0e19c3e46cc11aa8c0a4c00446c97
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Device Details

"Thermo Fisher Scientific" Rotavirus Antigen Rapid Test (Non-sterile)
TW: "่ณฝ้ป˜้ฃ›ไธ–็ˆพ็ง‘ๆŠ€" ่ผช็‹€็—…ๆฏ’ๆŠ—ๅŽŸๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

8fe0e19c3e46cc11aa8c0a4c00446c97

Ministry of Health Medical Device Import No. 017174

DHA09401717408

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Polio Virus Serological Reagent (C.3405)".

C Immunology and microbiology devices

C3405 Polio virus serum reagent

Imported from abroad

Dates and Status

Nov 14, 2016

Nov 14, 2021