Taiwan FDA registration 18f3d022bc6482ee57b607b3fb941e5f
"TIAS" Mini Whisky Automatic Red Blood Cell Sedimentation Rate Device (Unsterilized)
TW: "蒂艾思" 迷你威士美 自動紅血球沉降速率裝置 (未滅菌)
Taiwan·Risk Class 1·DIESSE DIAGNOSTICA SENESE S.P.A.·Registered Jun 24, 2011 – Jun 24, 2016CancelledRegistration details
- Analysis ID
- 18f3d022bc6482ee57b607b3fb941e5f
- Customs Code
- DHA04401051506
Company information
- Manufacturer
- DIESSE DIAGNOSTICA SENESE S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- GRANT TECHNOLOGY 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 24, 2011
- Expiry Date
- Jun 24, 2016
- Cancellation Date
- May 10, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "TIAS" Mini Whisky Automatic Red Blood Cell 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 18f3d022bc6482ee57b607b3fb941e5f and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRANT TECHNOLOGY CO., LTD..
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