"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..
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.
Device Details
Registration Details
ff83cf5af87186bdf01ad1224b5e3140
DHA08401785000
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

