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"PRF" Automated Sedimentation Rate Device (Non-Sterile) - Taiwan Registration 223d1aaf9446c6544f9b896bee7db7bd

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 223d1aaf9446c6544f9b896bee7db7bd and manufactured by SARL PROCESS FOR PRF. The authorized representative in Taiwan is ADENT MED 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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223d1aaf9446c6544f9b896bee7db7bd
Registration Details
Taiwan FDA Registration: 223d1aaf9446c6544f9b896bee7db7bd
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Device Details

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

Registration Details

223d1aaf9446c6544f9b896bee7db7bd

Ministry of Health Medical Device Import No. 016247

DHA09401624704

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 11, 2016

Mar 11, 2021

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