Taiwan FDA registration 3fa30318a483de40517a65d4c922953f
“SOPHYSA” Pressio ICP Monitoring System
TW: “索菲沙”顱內壓監視器及附件
Taiwan·Risk Class 2·MD·SOPHYSA·Registered Dec 16, 2015 – Dec 16, 2020CancelledRegistration details
- Analysis ID
- 3fa30318a483de40517a65d4c922953f
- License Form
- Ministry of Health Medical Device Import No. 028017
- Customs Code
- DHA05602801709
Company information
- Manufacturer
- SOPHYSA
- Manufacturer Country
- France
- Authorized Representative
- BARRY TEC ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K1620 Intracranial Pressure Monitor Material
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 16, 2015
- Expiry Date
- Dec 16, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “SOPHYSA” Pressio ICP Monitoring System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3fa30318a483de40517a65d4c922953f and manufactured by SOPHYSA. The authorized representative in Taiwan is BARRY TEC ENTERPRISE CO., LTD..
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