Taiwan FDA registration f05f32571436ea1520de47d84419bc31

"Philips" X-ray system

TW: “飛利浦”X光系統
Taiwan flagTaiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS DMC GMBH;; PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Registered Sep 20, 2017 – Sep 20, 2027Active
Registration details
Analysis ID
f05f32571436ea1520de47d84419bc31
Customs Code
DHAS5603025502
Company information
Manufacturer Country
Germany;;Netherlands
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
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.1650 透視X光影像增感管
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
Sep 20, 2017
Expiry Date
Sep 20, 2027
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About this record

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 f05f32571436ea1520de47d84419bc31 and manufactured by PHILIPS MEDICAL SYSTEMS DMC GMBH;; 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.

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