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"healgen" influenza A&B rapid test (Non-Sterile) - Taiwan Registration de0c6a13a8997e210161ed5c88d0a2af

Access comprehensive regulatory information for "healgen" influenza 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 de0c6a13a8997e210161ed5c88d0a2af and manufactured by HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANY. The authorized representative in Taiwan is MIN JIER FIRM.

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de0c6a13a8997e210161ed5c88d0a2af
Registration Details
Taiwan FDA Registration: de0c6a13a8997e210161ed5c88d0a2af
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Device Details

"healgen" influenza A&B rapid test (Non-Sterile)
TW: "ๅŸบๅ› " A/B ๅž‹ๆตๆ„Ÿๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

de0c6a13a8997e210161ed5c88d0a2af

Ministry of Health Medical Device Import No. 016255

DHA09401625503

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

Mar 14, 2016

Mar 14, 2021