Taiwan FDA registration 10610b1fd4075c9dab931792fa46559a
"Philips" multifunctional digital X-ray system
TW: “飛利浦”多功能數位X光系統
Taiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS DMC GMBH·Registered Jul 16, 2007 – Jul 16, 2017CancelledRegistration details
- Analysis ID
- 10610b1fd4075c9dab931792fa46559a
- Customs Code
- DHAS0601816405
Company information
- Manufacturer
- PHILIPS MEDICAL SYSTEMS DMC GMBH
- Manufacturer Country
- Germany
- 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.1680 固定式X光系統
- Import Information
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
- Registration Date
- Jul 16, 2007
- Expiry Date
- Jul 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" multifunctional digital X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 10610b1fd4075c9dab931792fa46559a and manufactured by PHILIPS MEDICAL SYSTEMS DMC GMBH. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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