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“B&E”Base Plate Shellac (Non-Sterile) - Taiwan Registration 2ab3af58204b714209cf7dce39d634be

Access comprehensive regulatory information for “B&E”Base Plate Shellac (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2ab3af58204b714209cf7dce39d634be and manufactured by B&E KOREA CO., LTD. The authorized representative in Taiwan is Mi Luo International Limited Company.

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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2ab3af58204b714209cf7dce39d634be
Registration Details
Taiwan FDA Registration: 2ab3af58204b714209cf7dce39d634be
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Device Details

“B&E”Base Plate Shellac (Non-Sterile)
TW: “比隱依”基底塗料 (未滅菌)
Risk Class 1
MD

Registration Details

2ab3af58204b714209cf7dce39d634be

Ministry of Health Medical Device Import No. 021627

DHA09402162708

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of base coatings (F.6200) of the medical equipment management measures.

F Dental devices

F6200 base coating

Imported from abroad

Dates and Status

Jun 11, 2020

Jun 11, 2025