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SEBIA CAPILLARYS CDT (Non-Sterile) - Taiwan Registration 2aeb51f8af57a151392221c278dfd72d

Access comprehensive regulatory information for SEBIA CAPILLARYS CDT (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 2aeb51f8af57a151392221c278dfd72d and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..

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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2aeb51f8af57a151392221c278dfd72d
Registration Details
Taiwan FDA Registration: 2aeb51f8af57a151392221c278dfd72d
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Device Details

SEBIA CAPILLARYS CDT (Non-Sterile)
TW: ่ณฝๆฏ”ไบž ๆฏ›็ดฐ็ฎก็ผบ้†ฃๆ”œ้ต่›‹็™ฝๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2aeb51f8af57a151392221c278dfd72d

Ministry of Health Medical Device Import No. 022538

DHA09402253801

Company Information

France

Product Details

Limited to the first level identification range of the measures for the administration of medical devices "r-glutamyl transferase (GGT) and isoenzyme test system (A.1360)".

A Clinical chemistry and clinical toxicology

A1360 r-glutamyl transferase (GGT) and isoenzyme test system

Imported from abroad

Dates and Status

Apr 27, 2021

Apr 27, 2026