Taiwan FDA registration a743210b11b806e30218082b50f1eb42
"Philips" Diagnostic x-ray tube housing assembly (Non-Sterile)
TW: "飛利浦" 診斷用X光球管套組件 (未滅菌)
Taiwan·Risk Class 1·MD·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Registered Jul 11, 2016 – Jul 11, 2026ExpiredRegistration details
- Analysis ID
- a743210b11b806e30218082b50f1eb42
- License Form
- Ministry of Health Medical Device Import No. 016764
- Customs Code
- DHAS9401676406
Company information
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Manufacturer Country
- Netherlands
- 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 Devices for radiology
- Product Type (Level 2)
- P1760 X-ray tube sleeve assembly for diagnostics
- Import Information
- Imported from abroad; Consent must be attached to the input (each input must be supported by the consent of the Atomic Energy Commission)
Dates and status
- Registration Date
- Jul 11, 2016
- Expiry Date
- Jul 11, 2026
About this record
Access comprehensive regulatory information for "Philips" Diagnostic x-ray tube housing assembly (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a743210b11b806e30218082b50f1eb42 and manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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