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“SHOFU” GLASIONOMER FX ULTRA - Taiwan Registration bf5377ef9decbc6b07e983c8bb490295

Access comprehensive regulatory information for “SHOFU” GLASIONOMER FX ULTRA in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf5377ef9decbc6b07e983c8bb490295 and manufactured by SHOFU INC.. The authorized representative in Taiwan is SHOFU INC., TAIWAN BRANCH (JAPAN).

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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bf5377ef9decbc6b07e983c8bb490295
Registration Details
Taiwan FDA Registration: bf5377ef9decbc6b07e983c8bb490295
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Device Details

“SHOFU” GLASIONOMER FX ULTRA
TW: “松風”奧創玻璃離子充填材
Risk Class 2
MD

Registration Details

bf5377ef9decbc6b07e983c8bb490295

Ministry of Health Medical Device Import No. 029868

DHA05602986801

Company Information

Japan

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F3275 Dental cement (Sminting)

Imported from abroad

Dates and Status

May 26, 2017

May 26, 2027