Taiwan FDA registration 65d0e75cb4fe353f12274ca96443b57f

X-ray tube sleeve assembly for diagnostic "Dangli" (unsterilized)　

TW: “當立”診斷用X光球管套組件 (未滅菌)　

Taiwan·Risk Class 1·DUNLEE, A DIVISION OF PHILIPS MEDICAL SYSTEMS, CLEVELAND, INC·Registered Apr 29, 2009 – Apr 29, 2014Cancelled

Registration details

Analysis ID: 65d0e75cb4fe353f12274ca96443b57f
Customs Code: DHAS4400767500

Company information

Manufacturer: DUNLEE, A DIVISION OF PHILIPS MEDICAL SYSTEMS, CLEVELAND, INC
Manufacturer Country: United States
Authorized Representative: Defeng Technology Co., Ltd

Product details

Intended Use: Limited to the first-level identification range of the Measures for the Administration of Medical Devices "X-ray Tube Sleeve Components for Diagnosis (P.1760)".
Product Type (Level 1): P Radiology Science
Product Type (Level 2): P.1760 診斷用X光球管套組件
Import Information: Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input

Dates and status

Registration Date: Apr 29, 2009
Expiry Date: Apr 29, 2014
Cancellation Date: Sep 26, 2016

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for X-ray tube sleeve assembly for diagnostic "Dangli" (unsterilized)　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 65d0e75cb4fe353f12274ca96443b57f and manufactured by DUNLEE, A DIVISION OF PHILIPS MEDICAL SYSTEMS, CLEVELAND, INC. The authorized representative in Taiwan is Defeng Technology Co., Ltd.

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