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"PRF" Automated sedimentation rate device (NON-STERILE) - Taiwan Registration dd393b178e9a5b30895529bdf4d006ac

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 dd393b178e9a5b30895529bdf4d006ac and manufactured by PROCESS FOR PRF S.A.R.L. The authorized representative in Taiwan is SE-US 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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dd393b178e9a5b30895529bdf4d006ac
Registration Details
Taiwan FDA Registration: dd393b178e9a5b30895529bdf4d006ac
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Device Details

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

Registration Details

dd393b178e9a5b30895529bdf4d006ac

Ministry of Health Medical Device Import No. 015604

DHA09401560400

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

Aug 27, 2015

Aug 27, 2025

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