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Legionella latex agglutination kit (unsterilized) - Taiwan Registration 4ab0e082b5218d2f757e420a1c607cbb

Access comprehensive regulatory information for Legionella latex agglutination kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4ab0e082b5218d2f757e420a1c607cbb and manufactured by LIOFILCHEM S.R.L.. 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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4ab0e082b5218d2f757e420a1c607cbb
Registration Details
Taiwan FDA Registration: 4ab0e082b5218d2f757e420a1c607cbb
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Device Details

Legionella latex agglutination kit (unsterilized)
TW: ใ€็ซ‹้ฃ›ๆ—‹ใ€ž้€€ไผ่ปไบบๆกฟ่Œๅฑฌไนณ่† ๅ‡้›†่ฉฆๅŠ‘ๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4ab0e082b5218d2f757e420a1c607cbb

DHA04401077506

Company Information

Italy

Product Details

Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.

C Immunology and microbiology

C.3300 ๅ—œ่ก€ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Aug 30, 2011

Aug 30, 2016

May 28, 2018

Cancellation Information

Logged out

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