Taiwan FDA registration 5faf718f74301b0472fb200a2ea6fc1d
"Philips" diagnostic X-ray tube sleeve assembly (unsterilized)
TW: “飛利浦”診斷用X光球管套組件 (未滅菌)
Taiwan·Risk Class 1·PHILIPS MEDICAL SYSTEMS(CLEVELAND) INC., DUNLEE DIV OF PH. MEDICAL SYSTEMS·Registered Mar 16, 2009 – Mar 16, 2014CancelledRegistration details
- Analysis ID
- 5faf718f74301b0472fb200a2ea6fc1d
- Customs Code
- DHAS4400755401
Company information
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "X-ray Tube Sleeve Components for Diagnosis (P.1760)".
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1760 診斷用X光球管套組件
- Import Information
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
- Registration Date
- Mar 16, 2009
- Expiry Date
- Mar 16, 2014
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Philips" diagnostic X-ray tube sleeve assembly (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5faf718f74301b0472fb200a2ea6fc1d and manufactured by PHILIPS MEDICAL SYSTEMS(CLEVELAND) INC., DUNLEE DIV OF PH. MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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