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Airbi Blood Mixer and Blood Gravimetric Analysis Device (Unsterilized) - Taiwan Registration 4c1f6eb60759c4cf1d39910c6ca104af

Access comprehensive regulatory information for Airbi Blood Mixer and Blood Gravimetric Analysis Device (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4c1f6eb60759c4cf1d39910c6ca104af and manufactured by LMB Technologie GmbH. The authorized representative in Taiwan is AMAZING MEDICAL INC..

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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4c1f6eb60759c4cf1d39910c6ca104af
Registration Details
Taiwan FDA Registration: 4c1f6eb60759c4cf1d39910c6ca104af
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Device Details

Airbi Blood Mixer and Blood Gravimetric Analysis Device (Unsterilized)
TW: โ€œ่‰พ็ˆพ็•ขโ€ๅ€็พŽ่ก€ๆถฒๆททๅˆๅ™จๅŠ่ก€ๆถฒ้‡้‡ๅˆ†ๆž่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

4c1f6eb60759c4cf1d39910c6ca104af

DHA08402053400

Company Information

Germany

Product Details

It is limited to the first level of identification of the "Blood Mixer and Blood Gravimetric Analysis Device (B.9195)" of the Administrative Measures for the Classification and Grading of Medical Devices.

B Hematology, pathology, and genetics

B.9195 Blood Mixers and Blood Gravimetric Analysis Devices

Input;; QMS/QSD

Dates and Status

Oct 01, 2021

Oct 31, 2024