"NIHON KOHDEN" Blood cell diluent (Non-Sterile)
- Analysis ID
- 9362f37c65433fb36e40960b2ac7eb5c
- License Form
- Ministry of Health Medical Device Import No. 015819
- Customs Code
- DHA09401581905
- Manufacturer
- NIHON KOHDEN TOMIOKA CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- K&C MEDICAL CO., LTD.
- 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
- Registration Date
- Nov 04, 2015
- Expiry Date
- Nov 04, 2025
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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.