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"Mei Eliel" Baynex Staphylococcus aureus rapid diagnostic reagent (unsterilized) - Taiwan Registration d5de22d733848682829d7a136b7359f7

Access comprehensive regulatory information for "Mei Eliel" Baynex Staphylococcus aureus rapid diagnostic reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d5de22d733848682829d7a136b7359f7 and manufactured by ALERE SCARBOROUGH, INC.. The authorized representative in Taiwan is Ariel Health Inc.

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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d5de22d733848682829d7a136b7359f7
Registration Details
Taiwan FDA Registration: d5de22d733848682829d7a136b7359f7
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Device Details

"Mei Eliel" Baynex Staphylococcus aureus rapid diagnostic reagent (unsterilized)
TW: "็พŽ่‰พๅˆฉ็ˆพ"ๆ‹œๅฅˆๅ…‹ๆ€้‡‘้ปƒ่‰ฒ่‘ก่„็ƒ่Œๅฟซ้€Ÿ่จบๆ–ท่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d5de22d733848682829d7a136b7359f7

DHA04400875801

Company Information

United States

Product Details

Limited to the first level identification range of the "Staphylococcus aureus serum reagent (C.3700)" of the Measures for the Administration of Medical Devices.

C Immunology and microbiology

C.3700 ้‡‘้ปƒ่‰ฒ่‘ก่„็ƒ่Œ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Apr 22, 2010

Apr 22, 2020

Jul 15, 2022

Cancellation Information

Logged out

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