Taiwan FDA registration 3d1cf0f521df186df4dc50a0b5643315
"Philips" positron/magnetic imaging system
TW: “飛利浦”正子/磁振影像系統
Taiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.·Registered Jan 31, 2013 – Jan 31, 2018CancelledRegistration details
- Analysis ID
- 3d1cf0f521df186df4dc50a0b5643315
- Customs Code
- DHA00602440607
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.1200 Radiology CT system
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
- Registration Date
- Jan 31, 2013
- Expiry Date
- Jan 31, 2018
- 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" positron/magnetic imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3d1cf0f521df186df4dc50a0b5643315 and manufactured by PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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