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"PRF" Automated Sedimentation Rate Device (Non-Sterile) - Taiwan Registration 470e8c10f5360c3f7b2850acd158e071

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 470e8c10f5360c3f7b2850acd158e071 and manufactured by SARL PROCESS FOR PRF. The authorized representative in Taiwan is HON INTERNATIONAL TRADING 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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470e8c10f5360c3f7b2850acd158e071
Registration Details
Taiwan FDA Registration: 470e8c10f5360c3f7b2850acd158e071
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Device Details

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

Registration Details

470e8c10f5360c3f7b2850acd158e071

Ministry of Health Medical Device Import No. 018619

DHA09401861902

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

Dec 15, 2017

Dec 15, 2022

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