Taiwan FDA registration 903808cb8f3d28fb1a5686387678617f

"Varian" linear accelerator

TW: "瓦里安"直線加速器
Taiwan flagTaiwan·Risk Class 2·Varian Medical Systems China Co. Ltd.·Registered Feb 24, 2017 – Feb 24, 2022Cancelled
Registration details
Analysis ID
903808cb8f3d28fb1a5686387678617f
Customs Code
DHAS9200081602
Company information
Manufacturer Country
China
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.5050 Medical Charged Particle Radiotherapy System
Import Information
Input;; Chinese goods;; 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". 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
Feb 24, 2017
Expiry Date
Feb 24, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Varian" linear accelerator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 903808cb8f3d28fb1a5686387678617f and manufactured by Varian Medical Systems China Co. Ltd.. The authorized representative in Taiwan is Varian Medical Systems Taiwan Co., Ltd..

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including Varian Medical Systems Haan GmbH, Manufacturing Site Kemnath;; Varian Medical Systems, Inc, Varian Medical Systems UK Ltd., and 4 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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