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“Kereden” temporary gingival retraction (Non-sterile) - Taiwan Registration e53d77dddb493631a39629820a6df71d

Access comprehensive regulatory information for “Kereden” temporary gingival retraction (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 e53d77dddb493631a39629820a6df71d and manufactured by KEREDEN CO. LTD.. The authorized representative in Taiwan is LA FU INDUSTRIAL CO., LTD..

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e53d77dddb493631a39629820a6df71d
Registration Details
Taiwan FDA Registration: e53d77dddb493631a39629820a6df71d
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Device Details

“Kereden” temporary gingival retraction (Non-sterile)
TW: “克拉登” 暫時性排齦膏組 (未滅菌)
Risk Class 1
MD

Registration Details

e53d77dddb493631a39629820a6df71d

Ministry of Health Medical Device Import No. 020565

DHA09402056507

Company Information

France

Product Details

Limited to the first level identification range of the gingival line (F.0001) of the medical equipment management method.

F Dental devices

F0001 Gingival drain line

Imported from abroad

Dates and Status

Jun 18, 2019

Jun 18, 2024