Taiwan FDA registration 27399a0086a4c2dbb6f773a4a04b98c7

"DIASCOT" Touch Automatic Red Blood Cell Sedimentation Rate Meter (Unsterilized)

TW: “迪雅仕” 觸控式自動紅血球沉降速率儀 (未滅菌)

Taiwan·Risk Class 1·DIESSE DIAGNOSTICA SENESE S.P.A.·Registered Oct 11, 2018 – Oct 11, 2028Active

Registration details

Analysis ID: 27399a0086a4c2dbb6f773a4a04b98c7
Customs Code: DHA09401969701

Company information

Manufacturer: DIESSE DIAGNOSTICA SENESE S.P.A.
Manufacturer Country: Italy
Authorized Representative: GRAND MARQUIS CO., LTD.

Product details

Intended Use: It is limited to the first level of identification scope of the "Automatic Sedimentation Rate Device (B.5800)" of the Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.5800 Automatic settling rate device
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Oct 11, 2018
Expiry Date: Oct 11, 2028

About this record

Access comprehensive regulatory information for "DIASCOT" Touch Automatic Red Blood Cell Sedimentation Rate Meter (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 27399a0086a4c2dbb6f773a4a04b98c7 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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