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“Bisco” TheraCal LC Light-Cured Resin-Modified Calcium Silicate Pulp Protectant/Liner - Taiwan Registration 2410a5fb11540985d05a442a8a83986c

Access comprehensive regulatory information for “Bisco” TheraCal LC Light-Cured Resin-Modified Calcium Silicate Pulp Protectant/Liner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2410a5fb11540985d05a442a8a83986c and manufactured by BISCO, INC.. The authorized representative in Taiwan is KUO HWA DENTAL SUPPLIERS CO., LTD..

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2410a5fb11540985d05a442a8a83986c
Registration Details
Taiwan FDA Registration: 2410a5fb11540985d05a442a8a83986c
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Device Details

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

Registration Details

2410a5fb11540985d05a442a8a83986c

Ministry of Health Medical Device Import No. 026342

DHA05602634200

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

Jul 15, 2014

Jul 15, 2024