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and photocreatinine test system - Taiwan Registration 6193103dd8d267d36c701dd7e19bf8d1

Access comprehensive regulatory information for and photocreatinine 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 6193103dd8d267d36c701dd7e19bf8d1 and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. 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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6193103dd8d267d36c701dd7e19bf8d1
Registration Details
Taiwan FDA Registration: 6193103dd8d267d36c701dd7e19bf8d1
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Device Details

and photocreatinine test system
TW: ๅ’Œๅ…‰่‚Œ้…ธ้…่ฉฆ้ฉ—็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

6193103dd8d267d36c701dd7e19bf8d1

DHA00601591004

Company Information

Product Details

Quantitatively detect creatinine content in serum or urine.

A Clinical chemistry and clinical toxicology

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

import

Dates and Status

Jan 18, 2006

Jan 18, 2021

Oct 06, 2023

Cancellation Information

Logged out

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