Taiwan FDA registration a9379d86d5ed42a9f73dbd09644861ec

"Toshiba" magnetic resonance diagnostic device

TW: “東芝”磁振診斷裝置

Taiwan·Risk Class 2·TOSHIBA MEDICAL SYSTEMS CORPORATION·Registered May 13, 2014 – May 13, 2019Cancelled

Registration details

Analysis ID: a9379d86d5ed42a9f73dbd09644861ec
Customs Code: DHA05602620105

Company information

Manufacturer: TOSHIBA MEDICAL SYSTEMS CORPORATION
Manufacturer Country: Japan
Authorized Representative: ROTARY TRADING CO., LTD.

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.1000 磁振診斷裝置
Import Information: Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and status

Registration Date: May 13, 2014
Expiry Date: May 13, 2019
Cancellation Date: Jun 16, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Toshiba" magnetic resonance diagnostic device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a9379d86d5ed42a9f73dbd09644861ec and manufactured by TOSHIBA MEDICAL SYSTEMS CORPORATION. The authorized representative in Taiwan is ROTARY TRADING CO., LTD..

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