Taiwan FDA registration 2e35098667132d640d986e711c2977d2

"NIHON KOHDEN" Red cell lysing reagent (Non-Sterile)

TW: "光電" 紅血球溶解劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·NIHON KOHDEN TOMIOKA CORPORATION·Registered Jun 19, 2020 – Jun 19, 2025Expired
Registration details
Analysis ID
2e35098667132d640d986e711c2977d2
License Form
Ministry of Health Medical Device Import No. 021650
Customs Code
DHA09402165003
Company information
Manufacturer Country
Japan
Authorized Representative
CHFO BIOMED CORP.
Product details
Intended Use
Limited to the first level identification range of red blood cell dissolving agent (B.8540) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
B Hematology and pathology devices
Product Type (Level 2)
B8540 Red blood cell lytic
Import Information
Imported from abroad
Dates and status
Registration Date
Jun 19, 2020
Expiry Date
Jun 19, 2025
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Access comprehensive regulatory information for "NIHON KOHDEN" Red cell lysing reagent (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2e35098667132d640d986e711c2977d2 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, 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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