"Philips" diagnostic X-ray tube sleeve assembly (unsterilized)
Taiwan·Risk Class 1·SPELLMAN DE MEXICO, S.A. DE C.V. PLANTA 3·Registered Mar 13, 2019 – Mar 13, 2024Expired- Analysis ID
- 895292ddfbd328bdf2332131186a08b1
- Customs Code
- DHAS9402018202
- Manufacturer
- SPELLMAN DE MEXICO, S.A. DE C.V. PLANTA 3
- Manufacturer Country
- Mexico
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- Limited to the first level identification range of the "X-ray tube sleeve assembly for diagnosis (P.1760)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1760 診斷用X光球管套組件
- 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
- Mar 13, 2019
- Expiry Date
- Mar 13, 2024
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Access comprehensive regulatory information for "Philips" diagnostic X-ray tube sleeve assembly (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 895292ddfbd328bdf2332131186a08b1 and manufactured by SPELLMAN DE MEXICO, S.A. DE C.V. PLANTA 3. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including PHILIPS MEDICAL SYSTEMS DMC GMBH, GILARDONI S.P.A., 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.