Taiwan FDA registration 745c9319fe5c5e0ffc9876dbddd49a5c

"Dunley" diagnostic X-ray tube sleeve assembly (unsterilized)

TW: "敦立" 診斷用X光球管套組件 (未滅菌)

Taiwan·Risk Class 1·DUNLEE·Registered Aug 08, 2007 – Aug 08, 2012Cancelled

Registration details

Analysis ID: 745c9319fe5c5e0ffc9876dbddd49a5c
Customs Code: DHAS4400607408

Company information

Manufacturer: DUNLEE
Manufacturer Country: United States
Authorized Representative: BENQ MEDICAL TECHNOLOGY CORPORATION

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: 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: Aug 08, 2007
Expiry Date: Aug 08, 2012
Cancellation Date: Apr 30, 2014

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Dunley" diagnostic X-ray tube sleeve assembly (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 745c9319fe5c5e0ffc9876dbddd49a5c and manufactured by DUNLEE. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.

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