Pure Global

Shinohara uric acid test reagent - Taiwan Registration 32e0aeb37185abbabde467c532d6486e

Access comprehensive regulatory information for Shinohara uric acid test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 32e0aeb37185abbabde467c532d6486e and manufactured by SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER. The authorized representative in Taiwan is BEAM INTERNATIONAL 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
32e0aeb37185abbabde467c532d6486e
Registration Details
Taiwan FDA Registration: 32e0aeb37185abbabde467c532d6486e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Shinohara uric acid test reagent
TW: ็ญฑๅŽŸๅฐฟ้…ธๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

32e0aeb37185abbabde467c532d6486e

DHA04400931307

Company Information

Product Details

Limited to the first level identification range of the "uric acid test system (A.1775)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A.1775 ๅฐฟ้…ธ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Oct 06, 2010

Oct 06, 2015

May 17, 2018

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ