Tokuhiko in vitro diagnostic blood bank centrifuge (unsterilized)
- Analysis ID
- 583910855f9616560e69248c2034875c
- Manufacturer
- Deyan Medical Technology Instrument Co., Ltd.; Deyan Medical Technology Instrument Co., Ltd. Factory 1
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DIGISYSTEM LABORATORY INSTRUMENTS INC.
- 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
- Registration Date
- Oct 08, 2018
- Expiry Date
- Oct 08, 2023
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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.