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"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.

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b6779d2a97075e5d01d41cd92b04a52d
Registration Details
Taiwan FDA Registration: b6779d2a97075e5d01d41cd92b04a52d
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Device Details

"NIHON KOHDEN" Blood cell diluent (Non-Sterile)
TW: "ๅ…‰้›ป" ่ก€็ƒ็จ€้‡‹ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

b6779d2a97075e5d01d41cd92b04a52d

Ministry of Health Medical Device Import No. 021649

DHA09402164905

Company Information

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

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