"Philips" X-ray system
- Analysis ID
- 932d21eee0708b53a8cecef0a260ea7b
- Customs Code
- DHAS5603723900
- Manufacturer Country
- Netherlands;;India
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1650 透視X光影像增感管
- Import Information
- The consent of the Nuclear Safety Commission must be obtained for each import of this medical device.;; input
- Registration Date
- Jun 23, 2024
- Expiry Date
- Jun 23, 2029
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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 932d21eee0708b53a8cecef0a260ea7b and manufactured by Philips India limited;; 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 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.