Taiwan FDA registration 20431118b18863d9c886ac8b0a62543d

"Philips" cardiovascular X-ray system

TW: “飛利浦”心血管X光系統
Taiwan flagTaiwan·Risk Class 2·Philips Medical Systems Nederland B.V.·Registered Sep 28, 2018 – Sep 28, 2028Active
Registration details
Analysis ID
20431118b18863d9c886ac8b0a62543d
Customs Code
DHAS5603153701
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.1600 X-ray Vascular Photography System;; P.1650 Fluoroscopic X-ray Sensory Tube
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
Sep 28, 2018
Expiry Date
Sep 28, 2028
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About this record

Access comprehensive regulatory information for "Philips" cardiovascular 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 20431118b18863d9c886ac8b0a62543d 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, 2 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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