Taiwan FDA registration afd082f8e78121af92b0e2f2f2f419ed
"Philips" radiation therapy simulation planning system
TW: “飛利浦” 放射治療模擬計畫系統
Taiwan·Risk Class 1·PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.·Registered Aug 16, 2012 – Aug 16, 2017CancelledRegistration details
- Analysis ID
- afd082f8e78121af92b0e2f2f2f419ed
- Customs Code
- DHA00602393006
Company information
- Manufacturer
- PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.5840 Radiation therapy simulation system
- Import Information
- import
Dates and status
- Registration Date
- Aug 16, 2012
- Expiry Date
- Aug 16, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Philips" radiation therapy simulation planning system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number afd082f8e78121af92b0e2f2f2f419ed and manufactured by PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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