"NIHON KOHDEN" Blood cell diluent (Non-Sterile) - Taiwan Registration b6779d2a97075e5d01d41cd92b04a52d
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.
Device Details
Registration Details
b6779d2a97075e5d01d41cd92b04a52d
Ministry of Health Medical Device Import No. 021649
DHA09402164905
Product Details
Limited to the first level identification range of blood cell thinners (B.8200) of the management methods for medical devices.
B Hematology and pathology devices
B8200 Blood cell thinner
Imported from abroad
Dates and Status
Jun 19, 2020
Jun 19, 2025

