Taiwan FDA registration b6779d2a97075e5d01d41cd92b04a52d

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

TW: "光電" 血球稀釋劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·NIHON KOHDEN TOMIOKA CORPORATION·Registered Jun 19, 2020 – Jun 19, 2025Expired
Registration details
Analysis ID
b6779d2a97075e5d01d41cd92b04a52d
License Form
Ministry of Health Medical Device Import No. 021649
Customs Code
DHA09402164905
Company information
Manufacturer Country
Japan
Authorized Representative
CHFO BIOMED CORP.
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
Jun 19, 2020
Expiry Date
Jun 19, 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 b6779d2a97075e5d01d41cd92b04a52d 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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