Taiwan FDA registration d7e97b2cdad75e74e30a38b54d4c6357

"ZEISS" intraoperative tumor radiation therapy system and accessories

TW: “蔡司”穎巧賓術中腫瘤放射治療系統及配件
Taiwan flagTaiwan·Risk Class 2·CARL ZEISS MEDITEC AG·Registered Jan 17, 2014 – Jan 17, 2024Expired
Registration details
Analysis ID
d7e97b2cdad75e74e30a38b54d4c6357
Customs Code
DHAS5602579205
Company information
Manufacturer Country
Germany
Authorized Representative
TAIWAN INSTRUMENT 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.5900 X光放射線治療系統
Import Information
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); 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
Jan 17, 2014
Expiry Date
Jan 17, 2024
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About this record

Access comprehensive regulatory information for "ZEISS" intraoperative tumor radiation therapy system and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d7e97b2cdad75e74e30a38b54d4c6357 and manufactured by CARL ZEISS MEDITEC AG. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..

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