Taiwan FDA registration d06e1ceacf313f76c1e98d0d6987f71c

"Varian" linear accelerator

TW: “瓦里安”直線加速器
Taiwan flagTaiwan·Risk Class 2·Varian Medical Systems UK Ltd.;; Varian Medical Systems, Inc·Registered Sep 20, 2019 – Nov 20, 2027Active
Registration details
Analysis ID
d06e1ceacf313f76c1e98d0d6987f71c
Customs Code
DHAS5603288200
Company information
Manufacturer Country
United Kingdom;;United States
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
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". Input;; 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
Sep 20, 2019
Expiry Date
Nov 20, 2027
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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 d06e1ceacf313f76c1e98d0d6987f71c and manufactured by Varian Medical Systems UK Ltd.;; Varian Medical Systems, Inc. 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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