Taiwan FDA registration 73fc49041e7836eab370aa04572bdc45

"Dias" mini automatic red blood cell sedimentation rate meter (unsterilized)

TW: “迪雅仕”迷你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 08, 2018 – Oct 08, 2028Active

Registration details

Analysis ID: 73fc49041e7836eab370aa04572bdc45
Customs Code: DHA09401968504

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 08, 2018
Expiry Date: Oct 08, 2028

About this record

Access comprehensive regulatory information for "Dias" mini 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 73fc49041e7836eab370aa04572bdc45 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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