Taiwan FDA registration 70c93c1d395debec5fa40b7ee90a1f82

"Philips" X-ray system

TW: “飛利浦” X光系統
Taiwan flagTaiwan·Risk Class 2·Philips India limited;; Philips Medical Systems Nederland B.V.·Registered Oct 30, 2023 – Oct 30, 2028Active
Registration details
Analysis ID
70c93c1d395debec5fa40b7ee90a1f82
Customs Code
DHAS5603664605
Company information
Manufacturer Country
Netherlands;;India
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
Details are as detailed as approved Chinese instructions
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 30, 2023
Expiry Date
Oct 30, 2028
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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 70c93c1d395debec5fa40b7ee90a1f82 and manufactured by Philips India limited;; 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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