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PRF Automated Sedimentation Rate Device (Non-Sterile) - Taiwan Registration cda2efd1b62d050c713c9acc5ccd4ee6

Access comprehensive regulatory information for PRF Automated Sedimentation Rate 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 cda2efd1b62d050c713c9acc5ccd4ee6 and manufactured by PROCESS FOR PRF S.A.R.L. The authorized representative in Taiwan is Bao sheng medical CO.,LTD.

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cda2efd1b62d050c713c9acc5ccd4ee6
Registration Details
Taiwan FDA Registration: cda2efd1b62d050c713c9acc5ccd4ee6
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Device Details

PRF Automated Sedimentation Rate Device (Non-Sterile)
TW: ็šฎ็ˆพๅฏŒ่‡ชๅ‹•ๆฒ‰้™้€Ÿ็އ่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

cda2efd1b62d050c713c9acc5ccd4ee6

Ministry of Health Medical Device Import No. 022377

DHA09402237703

Company Information

France

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Automatic Sedimentation Rate Device (B.5800)".

B Hematology and pathology devices

B5800 Automatic Settling Rate Device

Imported from abroad

Dates and Status

Mar 10, 2021

Mar 10, 2026