Taiwan FDA registration 901877658a153ce3fafdbf0fb2ba4edf

Philips pository/computed tomography system

TW: “飛利浦”正子/電腦斷層掃描系統
Taiwan flagTaiwan·Risk Class 2·Philips Medical Systems Technologies, Ltd.;; Philips Medical Systems Nederland B.V.·Registered Jul 04, 2018 – Jul 04, 2028Active
Registration details
Analysis ID
901877658a153ce3fafdbf0fb2ba4edf
Customs Code
DHAS5603082106
Company information
Manufacturer Country
Israel;;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.1200 Radiology CT system
Import Information
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
Dates and status
Registration Date
Jul 04, 2018
Expiry Date
Jul 04, 2028
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About this record

Access comprehensive regulatory information for Philips pository/computed tomography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 901877658a153ce3fafdbf0fb2ba4edf and manufactured by Philips Medical Systems Technologies, Ltd.;; Philips Medical Systems Nederland B.V.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC., and 2 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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