Taiwan FDA registration 4b94a2f5c65cfa2952f0faffc234ed32

"Philips" diagnostic X-ray tube sleeve assembly (unsterilized)

TW: "飛利浦" 診斷用X光球管套組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·PHILIPS MEDICAL SYSTEMS DMC GMBH·Registered Jul 03, 2018 – Jul 03, 2028Active
Registration details
Analysis ID
4b94a2f5c65cfa2952f0faffc234ed32
Customs Code
DHAS9401925500
Company information
Manufacturer Country
Germany
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
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
Dates and status
Registration Date
Jul 03, 2018
Expiry Date
Jul 03, 2028
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About this record

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 4b94a2f5c65cfa2952f0faffc234ed32 and manufactured by PHILIPS MEDICAL SYSTEMS DMC GMBH. 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 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.

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