"Philips" X-ray system
- Analysis ID
- 23df7e5a27add47fbb9186e40c59fd0f
- Customs Code
- DHAS0602416302
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- 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)
- Registration Date
- Nov 13, 2012
- Expiry Date
- Nov 13, 2017
- Cancellation Date
- Dec 13, 2019
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Philips" 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 23df7e5a27add47fbb9186e40c59fd0f and manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Philips Medical Systems Nederland B.V., Philips India limited;; Philips Medical Systems Nederland B.V., and 5 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.