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Sanmeng creatinine liquid test system - Taiwan Registration e8d0f36172aa328b14d629c2c353fe62

Access comprehensive regulatory information for Sanmeng creatinine liquid test system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e8d0f36172aa328b14d629c2c353fe62 and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER. The authorized representative in Taiwan is MEDICARE PRODUCTS 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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e8d0f36172aa328b14d629c2c353fe62
Registration Details
Taiwan FDA Registration: e8d0f36172aa328b14d629c2c353fe62
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Device Details

Sanmeng creatinine liquid test system
TW: ไธ‰็›Ÿ ่‚Œ้…ธ้…ๆถฒ้ซ”่ฉฆ้ฉ—็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

e8d0f36172aa328b14d629c2c353fe62

DHA00602074802

Product Details

็”จไพ†ๅœจ่‡ชๅ‹•่‡จๅบŠๅŒ–ๅญธๅˆ†ๆžๅ„€ไธŠ้ซ”ๅค–ๅฎš้‡ๆธฌๅฎšไบบ้ซ”่ก€ๆธ…ไธญ็š„่‚Œ้…ธ้…(Creatinine)

A Clinical chemistry and clinical toxicology

A.1225 ่‚Œๆฐจ้…ธ้…่ฉฆ้ฉ—็ณป็ตฑ(Creatininetestsystem)

import

Dates and Status

Dec 17, 2009

Dec 17, 2014

Apr 25, 2018

Cancellation Information

Logged out

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