"NIHON KOHDEN" Blood cell diluent (Non-Sterile)
- Analysis ID
- b6779d2a97075e5d01d41cd92b04a52d
- License Form
- Ministry of Health Medical Device Import No. 021649
- Customs Code
- DHA09402164905
- Manufacturer
- NIHON KOHDEN TOMIOKA CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- CHFO BIOMED CORP.
- 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
- Jun 19, 2020
- Expiry Date
- Jun 19, 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 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.