Taiwan FDA registration ba3605d404c478cf7d13b7b54a810300

"Philips" X-ray system

TW: “飛利浦”X光系統
Taiwan flagTaiwan·Risk Class 2·Philips Medical Systems Nederland B.V.·Registered Oct 13, 2020 – Oct 13, 2025Expired
Registration details
Analysis ID
ba3605d404c478cf7d13b7b54a810300
Customs Code
DHAS5603405205
Company information
Manufacturer Country
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
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
Oct 13, 2020
Expiry Date
Oct 13, 2025
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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 ba3605d404c478cf7d13b7b54a810300 and manufactured by 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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