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“Spacer” Light-curing temporary filling material - Taiwan Registration df8cb4bbd27606258d85b804a7a1026a

Access comprehensive regulatory information for “Spacer” Light-curing temporary filling material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df8cb4bbd27606258d85b804a7a1026a and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.

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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df8cb4bbd27606258d85b804a7a1026a
Registration Details
Taiwan FDA Registration: df8cb4bbd27606258d85b804a7a1026a
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Device Details

“Spacer” Light-curing temporary filling material
TW: “斯必特”暫時性填補牙材
Risk Class 2
MD

Registration Details

df8cb4bbd27606258d85b804a7a1026a

Ministry of Health Medical Device Import No. 031595

DHA05603159507

Company Information

Korea, Republic of

Product Details

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

F Dental devices

F3690 Resin tusk wood

Imported from abroad

Dates and Status

Sep 07, 2018

Sep 07, 2028