Taiwan FDA registration 583910855f9616560e69248c2034875c

Tokuhiko in vitro diagnostic blood bank centrifuge (unsterilized)

TW: 德彥體外診斷用血庫離心機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Deyan Medical Technology Instrument Co., Ltd.; Deyan Medical Technology Instrument Co., Ltd. Factory 1·Registered Oct 08, 2018 – Oct 08, 2023Cancelled
Registration details
Analysis ID
583910855f9616560e69248c2034875c
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.9275 Blood bank centrifuge for in vitro diagnostics
Import Information
Domestic;; Contract manufacturing
Dates and status
Registration Date
Oct 08, 2018
Expiry Date
Oct 08, 2023
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for Tokuhiko in vitro diagnostic blood bank centrifuge (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 583910855f9616560e69248c2034875c and manufactured by Deyan Medical Technology Instrument Co., Ltd.; Deyan Medical Technology Instrument Co., Ltd. Factory 1. The authorized representative in Taiwan is DIGISYSTEM LABORATORY INSTRUMENTS INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Deyan Medical Technology Instrument Co., Ltd.; Deyan Medical Technology Instrument Co., Ltd. Factory 1, and 1 recent registrations in the same category. 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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