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"NIHON KOHDEN" Blood cell diluent (Non-Sterile) - Taiwan Registration 9362f37c65433fb36e40960b2ac7eb5c

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.

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9362f37c65433fb36e40960b2ac7eb5c
Registration Details
Taiwan FDA Registration: 9362f37c65433fb36e40960b2ac7eb5c
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Device Details

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

Registration Details

9362f37c65433fb36e40960b2ac7eb5c

Ministry of Health Medical Device Import No. 015819

DHA09401581905

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

Nov 04, 2015

Nov 04, 2025

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