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"Leofisian" identification medium (sterilized) - Taiwan Registration 9d8a4955fa07db4efc91d17bb6715875

Access comprehensive regulatory information for "Leofisian" identification medium (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9d8a4955fa07db4efc91d17bb6715875 and manufactured by LIOFILCHEM S.R.L.. The authorized representative in Taiwan is DiaTech Technology 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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9d8a4955fa07db4efc91d17bb6715875
Registration Details
Taiwan FDA Registration: 9d8a4955fa07db4efc91d17bb6715875
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Device Details

"Leofisian" identification medium (sterilized)
TW: โ€œๅˆฉๅฅง่ฒๆฃฎโ€้‘‘ๅˆฅๅŸน้คŠๅŸบ(ๆป…่Œ)
Risk Class 1

Registration Details

9d8a4955fa07db4efc91d17bb6715875

DHA09402271000

Company Information

Italy

Product Details

Limited to the classification and grading management measures of medical equipment "Identification medium (C.2320)The first level identification range.

C Immunology and microbiology

C.2320 Differential culture media

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Dec 02, 2021

Dec 02, 2026