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“WFR” Aquaplast Splinting Materials (Non-sterile) - Taiwan Registration 81c74d77284801d185247299097eed6d

Access comprehensive regulatory information for “WFR” Aquaplast Splinting Materials (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 81c74d77284801d185247299097eed6d and manufactured by WFR/AQUAPLAST CORPORATION. The authorized representative in Taiwan is BOULDER ENTERPRISE CO., LTD..

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81c74d77284801d185247299097eed6d
Registration Details
Taiwan FDA Registration: 81c74d77284801d185247299097eed6d
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Device Details

“WFR” Aquaplast Splinting Materials (Non-sterile)
TW: “達弗亞”夾板原料 (未滅菌)
Risk Class 1
MD

Registration Details

81c74d77284801d185247299097eed6d

Ministry of Health Medical Device Import Registration No. 007425

DHA08400742505

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Splints for Non-Expanded Limbs (I.3910)".

I General and plastic surgical devices

I3910 Splints for non-inflated extremities

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2024