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"Inmeve" Bacterial Pneumonia 2-in-1 Test Kit (Unsterilized) - Taiwan Registration 927ed05de0b155a6b82e17ceb2862d25

Access comprehensive regulatory information for "Inmeve" Bacterial Pneumonia 2-in-1 Test 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 927ed05de0b155a6b82e17ceb2862d25 and manufactured by STATENS SERUM INSTITUT. 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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927ed05de0b155a6b82e17ceb2862d25
Registration Details
Taiwan FDA Registration: 927ed05de0b155a6b82e17ceb2862d25
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Device Details

"Inmeve" Bacterial Pneumonia 2-in-1 Test Kit (Unsterilized)
TW: "่Œต็พŽ่Š™" ็ดฐ่Œๆ€ง่‚บ็‚ŽไบŒๅˆไธ€ๆชขๆธฌ็ต„ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

927ed05de0b155a6b82e17ceb2862d25

DHA09401629706

Company Information

Denmark

Product Details

Limited to the management method of medical equipment, Haemophilus serological reagent (C.3300) and streptococcus serum reagent (C.3740) The first level identification range is limited.

C Immunology and microbiology

C.3300 ๅ—œ่ก€ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘;; C.3740 ้ˆ็ƒ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Mar 22, 2016

Mar 22, 2021

Aug 15, 2023

Cancellation Information

Logged out

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