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"Coris" Legionella K set (Non-Sterile) - Taiwan Registration e94f443f2f23a3c5ecb928e45606991d

Access comprehensive regulatory information for "Coris" Legionella K set (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 e94f443f2f23a3c5ecb928e45606991d and manufactured by CORIS BIOCONCEPT. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.

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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e94f443f2f23a3c5ecb928e45606991d
Registration Details
Taiwan FDA Registration: e94f443f2f23a3c5ecb928e45606991d
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Device Details

"Coris" Legionella K set (Non-Sterile)
TW: "็ง‘้‡Œๆ–ฏ" ้€€ไผ่ปไบบ่Œ้ซ”ๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

e94f443f2f23a3c5ecb928e45606991d

Ministry of Health Medical Device Import No. 015129

DHA09401512906

Company Information

Belgium

Product Details

C Immunology and microbiology devices

C3300 Haemophilus serology

Imported from abroad

Dates and Status

Apr 20, 2015

Apr 20, 2020

May 19, 2022

Cancellation Information

Logged out

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