Taiwan FDA registration aa280e6114350596c32dc8a5fa9bf10b

"Tonoki" diagnostic X-ray tube sleeve assembly (unsterilized)

TW: “東之”診斷用X光球管套組件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·TOSHIBA ELECTRON TUBES & DEVICES CO., LTD.·Registered Mar 12, 2007 – Mar 12, 2012Cancelled
Registration details
Analysis ID
aa280e6114350596c32dc8a5fa9bf10b
Customs Code
DHAS4400566105
Company information
Manufacturer Country
Japan
Authorized Representative
WITTECH CO., LTD.
Product details
Intended Use
Limited to the first-level identification range of the Measures for the Administration of Medical Devices "X-ray Tube Sleeve Components for Diagnosis (P.1760)".
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1760 診斷用X光球管套組件
Import Information
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
Registration Date
Mar 12, 2007
Expiry Date
Mar 12, 2012
Cancellation Date
Apr 15, 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 "Tonoki" diagnostic X-ray tube sleeve assembly (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aa280e6114350596c32dc8a5fa9bf10b and manufactured by TOSHIBA ELECTRON TUBES & DEVICES CO., LTD.. The authorized representative in Taiwan is WITTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TOSHIBA ELECTRON TUBES & DEVICES CO., LTD., 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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