Taiwan FDA registration 2585c0da41cbfd44eaf4267078a562d6

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

TW: "日本光電" 紅血球溶解劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·NIHON KOHDEN TOMIOKA CORPORATION·Registered Nov 04, 2015 – Nov 04, 2025Expired
Registration details
Analysis ID
2585c0da41cbfd44eaf4267078a562d6
License Form
Ministry of Health Medical Device Import No. 015820
Customs Code
DHA09401582003
Company information
Manufacturer Country
Japan
Authorized Representative
K&C MEDICAL CO., LTD.
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
Nov 04, 2015
Expiry Date
Nov 04, 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 2585c0da41cbfd44eaf4267078a562d6 and manufactured by NIHON KOHDEN TOMIOKA CORPORATION. The authorized representative in Taiwan is K&C MEDICAL 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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