Taiwan FDA registration ed5434f4e5800cae1eb8c9fdd8936bf3
"Philips" fluoroscopic X-ray system
TW: "飛利浦"透視X光系統
Taiwan·Risk Class 2·PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.·Registered Nov 03, 2006 – Nov 03, 2016CancelledRegistration details
- Analysis ID
- ed5434f4e5800cae1eb8c9fdd8936bf3
- Customs Code
- DHAS4200014409
Company information
- Manufacturer
- PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.
- Manufacturer Country
- China
- 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.1660 非透視X光影像增感管
- 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
- Nov 03, 2006
- Expiry Date
- Nov 03, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Philips" fluoroscopic 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 ed5434f4e5800cae1eb8c9fdd8936bf3 and manufactured by PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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