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"KIMA" Manual blood cell counting device (Non-Sterile) - Taiwan Registration 85ffe05966dbe359fe947ce5b7c5e8b5

Access comprehensive regulatory information for "KIMA" Manual blood cell counting device (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 85ffe05966dbe359fe947ce5b7c5e8b5 and manufactured by KIMA S.A.S.. The authorized representative in Taiwan is RAFA INTERNATIONAL CORP..

This page provides complete technical specifications, regulatory compliance details. 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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85ffe05966dbe359fe947ce5b7c5e8b5
Registration Details
Taiwan FDA Registration: 85ffe05966dbe359fe947ce5b7c5e8b5
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Device Details

"KIMA" Manual blood cell counting device (Non-Sterile)
TW: "ๅฅ‡้ฆฌ" ๆ‰‹ๅ‹•่ก€็ƒ่จˆๆ•ธ่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

85ffe05966dbe359fe947ce5b7c5e8b5

Ministry of Health Medical Device Import No. 016418

DHA09401641805

Company Information

Italy

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Manual Blood Cell Counting Device (B.6160)".

B Hematology and pathology devices

B6160 Manual blood counting device

Imported from abroad

Dates and Status

Apr 19, 2016

Apr 19, 2021