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"Sudi" leptospira antibody rapid test reagent (unsterilized) - Taiwan Registration c1adc9af410b9e63178ab96615494b7a

Access comprehensive regulatory information for "Sudi" leptospira antibody rapid test 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 c1adc9af410b9e63178ab96615494b7a and manufactured by STANDARD DIAGNOSTICS, 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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c1adc9af410b9e63178ab96615494b7a
Registration Details
Taiwan FDA Registration: c1adc9af410b9e63178ab96615494b7a
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Device Details

"Sudi" leptospira antibody rapid test reagent (unsterilized)
TW: โ€œ้€Ÿๅธโ€้‰ค็ซฏ่žบๆ—‹้ซ”ๆŠ—้ซ”ๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

c1adc9af410b9e63178ab96615494b7a

DHA04400908609

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the medical device management measures "Leptospira sera reagent (C.3350)".

C Immunology and microbiology

C.3350 ้‰ค็ซฏ่žบๆ—‹่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Aug 12, 2010

Aug 12, 2015

Apr 25, 2018

Cancellation Information

Logged out

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