Taiwan FDA registration 8e7f89b77a551a241e6d8c8388cf612a

"ZEISS" intraoperative tumor radiation therapy system and accessories

TW: “蔡司”術中腫瘤放射治療系統及配件
Taiwan flagTaiwan·Risk Class 2·CARL ZEISS MEDITEC AG·Registered Aug 14, 2019 – Aug 14, 2029Active
Registration details
Analysis ID
8e7f89b77a551a241e6d8c8388cf612a
Customs Code
DHA05603279201
Company information
Manufacturer Country
Germany
Authorized Representative
Carl Zeiss Co., Ltd. Taipei Branch
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
Input;; Contract manufacturing
Dates and status
Registration Date
Aug 14, 2019
Expiry Date
Aug 14, 2029
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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 8e7f89b77a551a241e6d8c8388cf612a and manufactured by CARL ZEISS MEDITEC AG. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CARL ZEISS MEDITEC AG, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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