Taiwan FDA registration 07a7baa978df6506f38eb0c3c4e71c4e

Deyan centrifuge

TW: 德彥離心機

Taiwan·Risk Class 1·DIGISYSTEM LABORATORY INSTRUMENTS INC.·Registered Mar 28, 2006 – Mar 28, 2011Cancelled

Registration details

Analysis ID: 07a7baa978df6506f38eb0c3c4e71c4e
Customs Code: DHY04300111103

Company information

Manufacturer: DIGISYSTEM LABORATORY INSTRUMENTS INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: DIGISYSTEM LABORATORY INSTRUMENTS INC.

Product details

Intended Use: The volume of red blood cells in the blood is measured by using the quantitative blood separation method to determine whether the total number of red blood cells in the patient is normal.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.6400 Hemocytometry device
Import Information: Domestic

Dates and status

Registration Date: Mar 28, 2006
Expiry Date: Mar 28, 2011
Cancellation Date: Nov 15, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Deyan centrifuge in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 07a7baa978df6506f38eb0c3c4e71c4e and manufactured by DIGISYSTEM LABORATORY INSTRUMENTS INC.. 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.