Taiwan FDA registration 9a2dd851fcc4bd0f67ab46c7ba791686

“Kuan yi” Personnel Lead Protective Device (Non-Sterile)

TW: “寬奕”個人用鉛防護設備(未滅菌)

Taiwan·Risk Class 1·MD·Kuanyi Instrument Co., Ltd·Registered Apr 25, 2022 – Apr 25, 2027Active

Registration details

Analysis ID: 9a2dd851fcc4bd0f67ab46c7ba791686
License Form: Ministry of Health Medical Device Manufacturing No. 009545

Company information

Manufacturer: Kuanyi Instrument Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Kuanyi Instrument Co., Ltd

Product details

Intended Use: Limited to the classification and grading management measures for medical equipment "Personal Protective Shield (P.6500)" the first level identification range.
Product Type (Level 1): P Radiology Science
Product Type (Level 2): P6500 Personal Shield
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Apr 25, 2022
Expiry Date: Apr 25, 2027

About this record

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.

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