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"New Foden" automatic sedimentation rate device (unsterilized) - Taiwan Registration 4220188c02b45346ca4109c24ff71880

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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4220188c02b45346ca4109c24ff71880
Registration Details
Taiwan FDA Registration: 4220188c02b45346ca4109c24ff71880
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Device Details

"New Foden" automatic sedimentation rate device (unsterilized)
TW: "ๆ–ฐ็ฆ็™ป" ่‡ชๅ‹•ๆฒ‰้™้€Ÿ็އ่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

4220188c02b45346ca4109c24ff71880

DHA04401044906

Company Information

Italy

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Automatic Sedimentation Rate Device (B.5800)".

B Hematology, pathology, and genetics

B.5800 Automatic settling rate device

import

Dates and Status

Jun 07, 2011

Jun 07, 2021

Sep 10, 2019