Taiwan FDA registration 25f8b3ee74371bd54d7881fde161f06d

Japan photoelectric automatic blood cell analyzer

TW: 日本光電 全自動血球分析儀
Taiwan flagTaiwan·Risk Class 2·NIHON KOHDEN CORPORATION·Registered Dec 19, 2006 – Dec 19, 2011Cancelled
Registration details
Analysis ID
25f8b3ee74371bd54d7881fde161f06d
Customs Code
DHA00601783704
Company information
Manufacturer Country
Japan
Authorized Representative
Jingxiang Co., Ltd
Product details
Intended Use
The instrument automatically calculates red blood cells, white blood cells and platelets, takes the last circulating blood as a sample, and uses flow cytometry electronic impedance method and semiconductor laser photoelectric measurement to measure the size and number of blood cells, and classify white blood cells for clinical diagnosis reference.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.5220 Automatic Differentiation Cell Counter
Import Information
import
Dates and status
Registration Date
Dec 19, 2006
Expiry Date
Dec 19, 2011
Cancellation Date
Oct 30, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for Japan photoelectric automatic blood cell analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25f8b3ee74371bd54d7881fde161f06d and manufactured by NIHON KOHDEN CORPORATION. The authorized representative in Taiwan is Jingxiang Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NIHON KOHDEN TOMIOKA CORPORATION, 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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