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"PRF" Automated sedimentation rate device (NON-STERILE) - Taiwan Registration 70849deac162543c35a4dc3373231374

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 70849deac162543c35a4dc3373231374 and manufactured by PROCESS FOR PRF S.A.R.L. The authorized representative in Taiwan is A SUN TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SARL PROCESS FOR PRF, PROCESS FOR PRF S.A.R.L, and 4 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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70849deac162543c35a4dc3373231374
Registration Details
Taiwan FDA Registration: 70849deac162543c35a4dc3373231374
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Device Details

"PRF" Automated sedimentation rate device (NON-STERILE)
TW: "็•ข็ˆพๅฏŒ" ่‡ชๅ‹•ๆฒ‰้™้€Ÿ็އ่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

70849deac162543c35a4dc3373231374

Ministry of Health Medical Device Import No. 016794

DHA09401679407

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

Jul 21, 2016

Jul 21, 2026

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