Pure Global

"Glennon" diagnostic X-ray tube sleeve assembly (unsterilized) - Taiwan Registration 567e6f266d2fd58a98c671695c24cb7a

Access comprehensive regulatory information for "Glennon" 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 567e6f266d2fd58a98c671695c24cb7a and manufactured by Canon Electron Tubes & Devices Co., Ltd.. The authorized representative in Taiwan is PO YE X-RAY MFG. CORP..

This page provides complete technical specifications, regulatory compliance details. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
567e6f266d2fd58a98c671695c24cb7a
Registration Details
Taiwan FDA Registration: 567e6f266d2fd58a98c671695c24cb7a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Glennon" diagnostic X-ray tube sleeve assembly (unsterilized)
TW: "ๅ˜‰่ƒฝ" ่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

567e6f266d2fd58a98c671695c24cb7a

DHAS9401975000

Company Information

Product Details

Limited to the first level identification range of the "X-ray tube sleeve assembly for diagnosis (P.1760)" of the Measures for the Classification and Grading Management of Medical Equipment.

P Radiology Science

P.1760 ่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ

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

Oct 30, 2018

Oct 30, 2023