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“Bisco” TheraCal LC Light-Cured Resin-Modified Calcium Silicate Pulp Liner - Taiwan Registration f5153a57e91f7d5101b59bdf93eb7fa4

Access comprehensive regulatory information for “Bisco” TheraCal LC Light-Cured Resin-Modified Calcium Silicate Pulp Liner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5153a57e91f7d5101b59bdf93eb7fa4 and manufactured by BISCO, INC.. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.

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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f5153a57e91f7d5101b59bdf93eb7fa4
Registration Details
Taiwan FDA Registration: f5153a57e91f7d5101b59bdf93eb7fa4
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Device Details

“Bisco” TheraCal LC Light-Cured Resin-Modified Calcium Silicate Pulp Liner
TW: “畢斯寇”光固化矽酸鈣襯底材
Risk Class 2
MD

Registration Details

f5153a57e91f7d5101b59bdf93eb7fa4

Ministry of Health Medical Device Import No. 031646

DHA05603164601

Company Information

United States

Product Details

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

F Dental devices

F3250 Calcium hydroxide cavity substrate

Imported from abroad

Dates and Status

Sep 28, 2018

Sep 28, 2028