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Deyan capillary blood collection tube (unsterilized) - Taiwan Registration 75b11b829b11e3c9d1ed1e3d839933fd

Access comprehensive regulatory information for Deyan capillary blood collection tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 75b11b829b11e3c9d1ed1e3d839933fd and manufactured by VITREX MEDICAL A/S. The authorized representative in Taiwan is DIGISYSTEM LABORATORY INSTRUMENTS 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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75b11b829b11e3c9d1ed1e3d839933fd
Registration Details
Taiwan FDA Registration: 75b11b829b11e3c9d1ed1e3d839933fd
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Device Details

Deyan capillary blood collection tube (unsterilized)
TW: ๅพทๅฝฅๆฏ›็ดฐ่ก€ๆถฒๆ”ถ้›†็ฎก(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

75b11b829b11e3c9d1ed1e3d839933fd

DHA04400940601

Company Information

Denmark

Product Details

It is limited to the first level of identification scope of the "Capillary Blood Collection Tube (B.6150)" of the Measures for the Classification and Grading of Medical Devices.

B Hematology, pathology, and genetics

B.6150 Capillary Blood Collection Tubes

import

Dates and Status

Oct 25, 2010

Oct 25, 2025