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"GHope" Legionella (Non-Sterile) - Taiwan Registration 64f7c6d1c5d02e977a2acbdf540e0f1d

Access comprehensive regulatory information for "GHope" Legionella (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 64f7c6d1c5d02e977a2acbdf540e0f1d and manufactured by EIKEN CHEMICAL CO., LTD.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY 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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64f7c6d1c5d02e977a2acbdf540e0f1d
Registration Details
Taiwan FDA Registration: 64f7c6d1c5d02e977a2acbdf540e0f1d
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Device Details

"GHope" Legionella (Non-Sterile)
TW: "็‚ฌๅˆ" ้€€ไผ่ปไบบ่‚บ็‚ŽๅฐฟๆถฒๆŠ—ๅŽŸๅฟซ้€Ÿ่จบๆ–ท่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

64f7c6d1c5d02e977a2acbdf540e0f1d

Ministry of Health Medical Device Import No. 019413

DHA09401941300

Company Information

Product Details

C Immunology and microbiology devices

C3300 Haemophilus serology

Imported from abroad

Dates and Status

Jul 25, 2018

Jul 25, 2023

Jan 28, 2019

Cancellation Information

Logged out

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