Taiwan FDA registration ea4af38da170685dc1f1f0cc1c170700

"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·GILARDONI S.P.A.·Registered Mar 19, 2019 – Mar 19, 2029Active
Registration details
Analysis ID
ea4af38da170685dc1f1f0cc1c170700
Customs Code
DHAS9402020501
Company information
Manufacturer
GILARDONI S.P.A.
Manufacturer Country
Italy
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
Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
Registration Date
Mar 19, 2019
Expiry Date
Mar 19, 2029
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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 ea4af38da170685dc1f1f0cc1c170700 and manufactured by GILARDONI S.P.A.. 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, 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.

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