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“NIHON KOHDEN” Automated Hematology Analyzer - Taiwan Registration b61406571a61466ddf33c16e2712d530

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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b61406571a61466ddf33c16e2712d530
Registration Details
Taiwan FDA Registration: b61406571a61466ddf33c16e2712d530
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Device Details

“NIHON KOHDEN” Automated Hematology Analyzer
TW: “日本光電”自動血液分析儀
Risk Class 2
MD

Registration Details

b61406571a61466ddf33c16e2712d530

Ministry of Health Medical Device Import No. 031122

DHA05603112203

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order.

B Hematology and pathology devices

B5200 Automated Cell Counter

Imported from abroad

Dates and Status

May 25, 2018

May 25, 2028

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