Pure Global

"DiaSys" Uric Acid FS TOOS (Non-Sterile) - Taiwan Registration d921c24502ffce6abf9d5c378d823a17

Access comprehensive regulatory information for "DiaSys" Uric Acid FS TOOS (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d921c24502ffce6abf9d5c378d823a17 and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
d921c24502ffce6abf9d5c378d823a17
Registration Details
Taiwan FDA Registration: d921c24502ffce6abf9d5c378d823a17
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"DiaSys" Uric Acid FS TOOS (Non-Sterile)
TW: "ๅพทไฟก" ๅฐฟ้…ธ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d921c24502ffce6abf9d5c378d823a17

Ministry of Health Medical Device Import No. 020692

DHA09402069201

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

A1775 Uric acid test system

Imported from abroad

Dates and Status

Jul 29, 2019

Jul 29, 2024