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“Cellumed” Unios DBM - Taiwan Registration a765ee01902a3a5a78542c65634a48b0

Access comprehensive regulatory information for “Cellumed” Unios DBM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a765ee01902a3a5a78542c65634a48b0 and manufactured by Cellumed Co., Ltd.. The authorized representative in Taiwan is Careplusone (Taiwan) Co., Ltd..

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.

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a765ee01902a3a5a78542c65634a48b0
Registration Details
Taiwan FDA Registration: a765ee01902a3a5a78542c65634a48b0
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Device Details

“Cellumed” Unios DBM
TW: “瑟諾美”優尼奧斯去礦化異體植骨
Risk Class 2
MD

Registration Details

a765ee01902a3a5a78542c65634a48b0

Ministry of Health Medical Device Import No. 035059

DHA05603505903

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3045 Absorbable calcium salt bone cavity filling device

Imported from abroad

Dates and Status

Nov 15, 2021

Nov 23, 2026