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"Response Biomedical" Flu A/B Rapid Test (Non-sterile) - Taiwan Registration 544c4ca8f1bee73db9a4280c004b7f5d

Access comprehensive regulatory information for "Response Biomedical" Flu A/B 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 544c4ca8f1bee73db9a4280c004b7f5d 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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544c4ca8f1bee73db9a4280c004b7f5d
Registration Details
Taiwan FDA Registration: 544c4ca8f1bee73db9a4280c004b7f5d
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Device Details

"Response Biomedical" Flu A/B Rapid Test (Non-sterile)
TW: "็‘ž้‚ฆ็”Ÿ้†ซ" A/Bๅž‹ๆต่กŒๆ€งๆ„Ÿๅ†’็—…ๆฏ’ๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

544c4ca8f1bee73db9a4280c004b7f5d

Ministry of Health Medical Device Import No. 016043

DHA09401604301

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".

C Immunology and microbiology devices

C3330 Influenza virus serum reagent

Imported from abroad

Dates and Status

Jan 05, 2016

Jan 05, 2021