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"RDA" diagnostic X-ray tube sleeve assembly (unsterilized) - Taiwan Registration 3c8e0f6c47f2b733b0b63e76fa93579f

Access comprehensive regulatory information for "RDA" 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 3c8e0f6c47f2b733b0b63e76fa93579f and manufactured by HANGZHOU KAILONG MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is PO YE X-RAY MFG. CORP..

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3c8e0f6c47f2b733b0b63e76fa93579f
Registration Details
Taiwan FDA Registration: 3c8e0f6c47f2b733b0b63e76fa93579f
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Device Details

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

Registration Details

3c8e0f6c47f2b733b0b63e76fa93579f

DHAS9600383205

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); Chinese goods;; input

Dates and Status

Jun 10, 2019

Jun 10, 2029