Taiwan FDA registration a0764333aadc5fbf2ac10c6766b24a5b

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 Sep 19, 2006 – Sep 19, 2016Cancelled
Registration details
Analysis ID
a0764333aadc5fbf2ac10c6766b24a5b
Customs Code
DHAS0601712707
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
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); Input;; A consent form is required for each entry (a consent letter from the approved hospital clinic of the Department is required for each entry)
Dates and status
Registration Date
Sep 19, 2006
Expiry Date
Sep 19, 2016
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
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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 a0764333aadc5fbf2ac10c6766b24a5b 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 Technologies, Ltd.;; Philips Medical Systems Nederland B.V., 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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