Taiwan FDA registration cb26604a1bbfe5fce63801aa706d661c

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

TW: "守雷"診斷用X光球管套組件(未滅菌)

Taiwan·Risk Class 1·SOURCE-RAY, INC.·Registered Sep 05, 2011 – Sep 05, 2016Cancelled

Registration details

Analysis ID: cb26604a1bbfe5fce63801aa706d661c
Customs Code: DHAS4401080204

Company information

Manufacturer: SOURCE-RAY, INC.
Manufacturer Country: United States
Authorized Representative: Taiwan Tengxie Biotechnology 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: Sep 05, 2011
Expiry Date: Sep 05, 2016
Cancellation Date: Aug 14, 2018

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 "lightning" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cb26604a1bbfe5fce63801aa706d661c and manufactured by SOURCE-RAY, INC.. The authorized representative in Taiwan is Taiwan Tengxie Biotechnology Co., Ltd.

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