"Philips" mobile X-ray system
- Analysis ID
- 31acbd172cc1cb1ba57fd1488d4709bd
- Customs Code
- DHAS5602620202
- Manufacturer
- TECHNIX S. P. A.
- Manufacturer Country
- Italy
- 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.1720 移動式X光系統
- Import Information
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
- Registration Date
- May 19, 2014
- Expiry Date
- May 19, 2019
- Cancellation Date
- Jul 15, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Philips" mobile 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 31acbd172cc1cb1ba57fd1488d4709bd and manufactured by TECHNIX S. P. A.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including TECHNIX S. P. A., Philips Medical Systems Nederland B.V., and 2 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.