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Konya multi-analytical calibration solution - Taiwan Registration ed6c77884a374430957754d2490cc310

Access comprehensive regulatory information for Konya multi-analytical calibration solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed6c77884a374430957754d2490cc310 and manufactured by KAMIYA BIOMEDICAL COMPANY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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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ed6c77884a374430957754d2490cc310
Registration Details
Taiwan FDA Registration: ed6c77884a374430957754d2490cc310
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Device Details

Konya multi-analytical calibration solution
TW: ็ง‘ๅฐผไบžๅคš้ …ๅˆ†ๆžๆ กๆญฃๆถฒ
Risk Class 2
Cancelled

Registration Details

ed6c77884a374430957754d2490cc310

DHA00601726501

Company Information

United States

Product Details

ๆญคK-ASSAYยฎๅคš้ …ๅˆ†ๆžๆ กๆญฃๆถฒไธป่ฆ็‚บฮฑ-1 AG,ฮฑ-1 AT, C3, C4, Haptoglobin, IgA, IgG, IgM, ๅŠ Transferrin. ๅˆฉ็”จๅ…็–ซๆฏ”ๆฟๆณ•ๅฎš้‡ๆธฌๅฎš(immunoturbidimetric assay)ๆ™‚ๆ‰€้œ€ไน‹ๆ กๆญฃๆถฒ.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

import

Dates and Status

Aug 09, 2006

Aug 09, 2021

Jun 29, 2022

Cancellation Information

Logged out

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