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Universal hydroxide apatite bone graft cement - Taiwan Registration f3cbcf026e2ec370cbfea46251067609

Access comprehensive regulatory information for Universal hydroxide apatite bone graft cement in Taiwan's medical device market through Pure Global AI's free database. is registered under number f3cbcf026e2ec370cbfea46251067609 and manufactured by LIFECORE BIOMEDUCAL, INC. ORAL RESTORATIVE DIVISION. The authorized representative in Taiwan is Bowling Drug Instruments 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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f3cbcf026e2ec370cbfea46251067609
Registration Details
Taiwan FDA Registration: f3cbcf026e2ec370cbfea46251067609
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Device Details

Universal hydroxide apatite bone graft cement
TW: ๅˆๆ™ฎ้ฉๆฐซๆฐง็ฃท็ฐ็Ÿณ้ชจ็งปๆค่† ๆณฅ
Cancelled

Registration Details

f3cbcf026e2ec370cbfea46251067609

DHA00600699804

Company Information

Product Details

The details are as detailed as the approved copy of the imitation label

0399 Other artificial function substitutes

import

Dates and Status

Sep 11, 1993

Sep 11, 1998

Aug 24, 2000

Cancellation Information

Logged out

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