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"Puyi" diagnostic X-ray tube sleeve assembly (unsterilized) - Taiwan Registration 53fc9e7cbbd9925ebf2692f19bb9cc20

Access comprehensive regulatory information for "Puyi" 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 53fc9e7cbbd9925ebf2692f19bb9cc20 and manufactured by PO YE X-RAY MFG. CORP.. 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.

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53fc9e7cbbd9925ebf2692f19bb9cc20
Registration Details
Taiwan FDA Registration: 53fc9e7cbbd9925ebf2692f19bb9cc20
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Device Details

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

Registration Details

53fc9e7cbbd9925ebf2692f19bb9cc20

Company Information

Taiwan, Province of China

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

Domestic

Dates and Status

Aug 14, 2014

Aug 14, 2024