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"Unified" new resin fiber pre-module (unsterilized) - Taiwan Registration ff83cf5af87186bdf01ad1224b5e3140

Access comprehensive regulatory information for "Unified" new resin fiber pre-module (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ff83cf5af87186bdf01ad1224b5e3140 and manufactured by DONG HAE MEDICAL CO., LTD. The authorized representative in Taiwan is GREAT KUEI TAI INC..

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ff83cf5af87186bdf01ad1224b5e3140
Registration Details
Taiwan FDA Registration: ff83cf5af87186bdf01ad1224b5e3140
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Device Details

"Unified" new resin fiber pre-module (unsterilized)
TW: "็ตฑๅˆ" ๆ–ฐๅž‹ๆจน่„‚็บ–็ถญ้ ๆจก็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

ff83cf5af87186bdf01ad1224b5e3140

DHA08401785000

Company Information

Korea, Republic of

Product Details

Limited to the first level recognition range of medical equipment classification and grading management measures limb equipment (O.3475).

o Physical Medical Sciences

O.3475 Limb fittings

import

Dates and Status

Oct 01, 2021

Oct 31, 2025