Taiwan FDA registration 75b11b829b11e3c9d1ed1e3d839933fd

Deyan capillary blood collection tube (unsterilized)

TW: 德彥毛細血液收集管(未滅菌)

Taiwan·Risk Class 1·VITREX MEDICAL A/S·Registered Oct 25, 2010 – Oct 25, 2025Expired

Registration details

Analysis ID: 75b11b829b11e3c9d1ed1e3d839933fd
Customs Code: DHA04400940601

Company information

Manufacturer: VITREX MEDICAL A/S
Manufacturer Country: Denmark
Authorized Representative: DIGISYSTEM LABORATORY INSTRUMENTS INC.

Product details

Intended Use: 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.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.6150 Capillary Blood Collection Tubes
Import Information: import

Dates and status

Registration Date: Oct 25, 2010
Expiry Date: Oct 25, 2025

About this record

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.