Taiwan FDA registration b61406571a61466ddf33c16e2712d530

“NIHON KOHDEN” Automated Hematology Analyzer

TW: “日本光電”自動血液分析儀
Taiwan flagTaiwan·Risk Class 2·MD·NIHON KOHDEN TOMIOKA CORPORATION·Registered May 25, 2018 – May 25, 2028Active
Registration details
Analysis ID
b61406571a61466ddf33c16e2712d530
License Form
Ministry of Health Medical Device Import No. 031122
Customs Code
DHA05603112203
Company information
Manufacturer Country
Japan
Authorized Representative
CHFO BIOMED CORP.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order.
Product Type (Level 1)
B Hematology and pathology devices
Product Type (Level 2)
B5200 Automated Cell Counter
Import Information
Imported from abroad
Dates and status
Registration Date
May 25, 2018
Expiry Date
May 25, 2028
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About this record

Access comprehensive regulatory information for “NIHON KOHDEN” Automated Hematology Analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b61406571a61466ddf33c16e2712d530 and manufactured by NIHON KOHDEN TOMIOKA CORPORATION. The authorized representative in Taiwan is CHFO BIOMED CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Nihon Kohden Tomioka Corporation Tomioka Production Center, 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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