Taiwan FDA registration 87403a38f8d232b46bc6250ecacc67d2

Autoclave generator for diagnostic X-ray machine (unsterilized)

TW: “醫蒙德”診斷用X光機高壓產生器(未滅菌)
Taiwan flagTaiwan·Risk Class 1·EMD TECHNOLOGIES, INC.·Registered Sep 07, 2007 – Sep 07, 2012Cancelled
Registration details
Analysis ID
87403a38f8d232b46bc6250ecacc67d2
Customs Code
DHAS4400614008
Company information
Manufacturer Country
Canada
Authorized Representative
Defeng Technology Co., Ltd
Product details
Intended Use
Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "X-ray Machine High Voltage Generator for Diagnosis (P.1700)".
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1700 診斷用X光機高壓產生器
Import Information
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); QMS/QSD;; input
Dates and status
Registration Date
Sep 07, 2007
Expiry Date
Sep 07, 2012
Cancellation Date
Apr 09, 2014
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 Autoclave generator for diagnostic X-ray machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 87403a38f8d232b46bc6250ecacc67d2 and manufactured by EMD TECHNOLOGIES, INC.. The authorized representative in Taiwan is Defeng Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including COMMUNICATIONS & POWER INDUSTRIES CANADA INC., and 3 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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