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Japan photoelectric automatic blood cell analyzer - Taiwan Registration b93b7d0c1eeef4db3ba43a476e0cf8f9

Access comprehensive regulatory information for Japan photoelectric automatic blood cell analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b93b7d0c1eeef4db3ba43a476e0cf8f9 and manufactured by NIHON KOHDEN TOMIOKA CORPORATION. The authorized representative in Taiwan is Jingxiang Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NIHON KOHDEN 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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b93b7d0c1eeef4db3ba43a476e0cf8f9
Registration Details
Taiwan FDA Registration: b93b7d0c1eeef4db3ba43a476e0cf8f9
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Device Details

Japan photoelectric automatic blood cell analyzer
TW: ๆ—ฅๆœฌๅ…‰้›ปๅ…จ่‡ชๅ‹•่ก€็ƒๅˆ†ๆžๅ„€
Risk Class 2
Cancelled

Registration Details

b93b7d0c1eeef4db3ba43a476e0cf8f9

DHA00602507706

Company Information

Product Details

This product is suitable for the detection of red blood cells, white blood cells and platelet counts and white blood cell classification in whole blood, including 23 parameters.

B Hematology, pathology, and genetics

B.5220 Automatic Differentiation Cell Counter

import

Dates and Status

Jun 27, 2013

Jun 27, 2018

Dec 20, 2019

Cancellation Information

Logged out

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