Taiwan FDA registration a1b61d57d3a779547a0752888b7ca1e3

"Dias" Automatic Red Blood Cell Sedimentation Rate Meter (Unsterilized)

TW: “迪雅仕” 全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, 2023Expired

Registration details

Analysis ID: a1b61d57d3a779547a0752888b7ca1e3
Customs Code: DHA09401969800

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, 2023

About this record

Access comprehensive regulatory information for "Dias" 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 a1b61d57d3a779547a0752888b7ca1e3 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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.