Taiwan FDA registration 948fc98f1942355e5a39340bc0506fc7

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(CLEVELAND),INC.·Registered Jun 28, 2013 – Jun 28, 2018Cancelled
Registration details
Analysis ID
948fc98f1942355e5a39340bc0506fc7
Customs Code
DHAS0602498709
Company information
Manufacturer Country
United States
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
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
Jun 28, 2013
Expiry Date
Jun 28, 2018
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 948fc98f1942355e5a39340bc0506fc7 and manufactured by PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.. 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(CLEVELAND),INC., Philips Medical Systems Technologies, Ltd.;; Philips Medical Systems Nederland B.V., 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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