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“Kuan yi” Personnel Lead Protective Device (Non-Sterile) - Taiwan Registration 9a2dd851fcc4bd0f67ab46c7ba791686

Access comprehensive regulatory information for “Kuan yi” Personnel Lead Protective Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9a2dd851fcc4bd0f67ab46c7ba791686 and manufactured by Kuanyi Instrument Co., Ltd. The authorized representative in Taiwan is Kuanyi Instrument Co., Ltd.

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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9a2dd851fcc4bd0f67ab46c7ba791686
Registration Details
Taiwan FDA Registration: 9a2dd851fcc4bd0f67ab46c7ba791686
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Device Details

“Kuan yi” Personnel Lead Protective Device (Non-Sterile)
TW: “寬奕”個人用鉛防護設備(未滅菌)
Risk Class 1
MD

Registration Details

9a2dd851fcc4bd0f67ab46c7ba791686

Ministry of Health Medical Device Manufacturing No. 009545

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management measures for medical equipment "Personal Protective Shield (P.6500)" the first level identification range.

P Radiology Science

P6500 Personal Shield

Produced in Taiwan, China

Dates and Status

Apr 25, 2022

Apr 25, 2027