Taiwan FDA registration 9362f37c65433fb36e40960b2ac7eb5c

"NIHON KOHDEN" Blood cell diluent (Non-Sterile)

TW: "日本光電" 血球稀釋劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·NIHON KOHDEN TOMIOKA CORPORATION·Registered Nov 04, 2015 – Nov 04, 2025Expired
Registration details
Analysis ID
9362f37c65433fb36e40960b2ac7eb5c
License Form
Ministry of Health Medical Device Import No. 015819
Customs Code
DHA09401581905
Company information
Manufacturer Country
Japan
Authorized Representative
K&C MEDICAL CO., LTD.
Product details
Intended Use
Limited to the first level identification range of blood cell thinners (B.8200) of the management methods for medical devices.
Product Type (Level 1)
B Hematology and pathology devices
Product Type (Level 2)
B8200 Blood cell thinner
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 04, 2015
Expiry Date
Nov 04, 2025
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About this record

Access comprehensive regulatory information for "NIHON KOHDEN" Blood cell diluent (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 9362f37c65433fb36e40960b2ac7eb5c 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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