Taiwan FDA registration 887683155dcc8d58dbbcdb47464920ac

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

TW: “艾恩迪”診斷用X光球管套組件 (未滅菌)

Taiwan·Risk Class 1·IMD GENERATORS SRL·Registered Jan 13, 2012 – Jan 13, 2022Cancelled

Registration details

Analysis ID: 887683155dcc8d58dbbcdb47464920ac
Customs Code: DHAS4401129505

Company information

Manufacturer: IMD GENERATORS SRL
Manufacturer Country: Italy
Authorized Representative: INNOMED INTERNATIONAL INC.

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: Jan 13, 2012
Expiry Date: Jan 13, 2022
Cancellation Date: Apr 12, 2024

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 "ENDI" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 887683155dcc8d58dbbcdb47464920ac and manufactured by IMD GENERATORS SRL. The authorized representative in Taiwan is INNOMED INTERNATIONAL INC..

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