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"PROCESS" Automated sedimentation rate device (Non-Sterile) - Taiwan Registration c5673b24298839543d53dc804d4d2317

Access comprehensive regulatory information for "PROCESS" 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 c5673b24298839543d53dc804d4d2317 and manufactured by PROCESS FOR PRF S.A.R.L. The authorized representative in Taiwan is SMART LIFE INTERNATIONAL CO., LTD..

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c5673b24298839543d53dc804d4d2317
Registration Details
Taiwan FDA Registration: c5673b24298839543d53dc804d4d2317
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Device Details

"PROCESS" Automated sedimentation rate device (Non-Sterile)
TW: "ๆ™ฎๆ‹‰ๆ–ฏ" ่‡ชๅ‹•ๆฒ‰้™้€Ÿ็އ่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c5673b24298839543d53dc804d4d2317

Ministry of Health Medical Device Import No. 017779

DHA09401777903

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

May 02, 2017

May 02, 2022