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"Response Biomedical" RSV Rapid Test (non-sterile) - Taiwan Registration af7b00ad723ba5e16d2acd0a9dea70aa

Access comprehensive regulatory information for "Response Biomedical" RSV 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 af7b00ad723ba5e16d2acd0a9dea70aa and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI 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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af7b00ad723ba5e16d2acd0a9dea70aa
Registration Details
Taiwan FDA Registration: af7b00ad723ba5e16d2acd0a9dea70aa
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Device Details

"Response Biomedical" RSV Rapid Test (non-sterile)
TW: "็‘ž้‚ฆ็”Ÿ้†ซ" ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’ๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

af7b00ad723ba5e16d2acd0a9dea70aa

Ministry of Health Medical Device Import No. 016044

DHA09401604403

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Respiratory Fusion Cell Virus Serological Reagent (C.3480)".

C Immunology and microbiology devices

C3480 Respiratory Fusion Cell Virus Serological Reagent

Imported from abroad

Dates and Status

Jan 05, 2016

Jan 05, 2021