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"PRF" Automated Sedimentation Rate Device (Non-Sterile) - Taiwan Registration 3bc66fb2146d29cc3bc4284a8e409129

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 3bc66fb2146d29cc3bc4284a8e409129 and manufactured by SARL PROCESS FOR PRF. The authorized representative in Taiwan is CONTROL BIOTECH 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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3bc66fb2146d29cc3bc4284a8e409129
Registration Details
Taiwan FDA Registration: 3bc66fb2146d29cc3bc4284a8e409129
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Device Details

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

Registration Details

3bc66fb2146d29cc3bc4284a8e409129

Ministry of Health Medical Device Import No. 015683

DHA09401568306

Company Information

France

Product Details

B Hematology and pathology devices

B5800 Automatic Settling Rate Device

Imported from abroad

Dates and Status

Sep 17, 2015

Sep 17, 2020

Jun 22, 2022

Cancellation Information

Logged out

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