Taiwan FDA registration 4220188c02b45346ca4109c24ff71880

"New Foden" automatic sedimentation rate device (unsterilized)

TW: "新福登" 自動沉降速率裝置(未滅菌)

Taiwan·Risk Class 1·SILFRADENT S.R.L.·Registered Jun 07, 2011 – Jun 07, 2021Expired

Registration details

Analysis ID: 4220188c02b45346ca4109c24ff71880
Customs Code: DHA04401044906

Company information

Manufacturer: SILFRADENT S.R.L.
Manufacturer Country: Italy
Authorized Representative: BIOTECH MEDICAL SCIENCE 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, pathology, and genetics
Product Type (Level 2): B.5800 Automatic settling rate device
Import Information: import

Dates and status

Registration Date: Jun 07, 2011
Expiry Date: Jun 07, 2021
Cancellation Date: Sep 10, 2019

About this record

Access comprehensive regulatory information for "New Foden" automatic sedimentation rate device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4220188c02b45346ca4109c24ff71880 and manufactured by SILFRADENT S.R.L.. The authorized representative in Taiwan is BIOTECH MEDICAL SCIENCE CO., LTD..

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