Taiwan FDA registration c5673b24298839543d53dc804d4d2317

"PROCESS" Automated sedimentation rate device (Non-Sterile)

TW: "普拉斯" 自動沉降速率裝置 (未滅菌)

Taiwan·Risk Class 1·MD·PROCESS FOR PRF S.A.R.L·Registered May 02, 2017 – May 02, 2022Expired

Registration details

Analysis ID: c5673b24298839543d53dc804d4d2317
License Form: Ministry of Health Medical Device Import No. 017779
Customs Code: DHA09401777903

Company information

Manufacturer: PROCESS FOR PRF S.A.R.L
Manufacturer Country: France
Authorized Representative: SMART LIFE INTERNATIONAL CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Automatic Sedimentation Rate Device (B.5800)".
Product Type (Level 1): B Hematology and pathology devices
Product Type (Level 2): B5800 Automatic Settling Rate Device
Import Information: Imported from abroad

Dates and status

Registration Date: May 02, 2017
Expiry Date: May 02, 2022

About this record

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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