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"Reted" fiberglass root column (unsterilized) - Taiwan Registration de733a9acfbd37a46cf7b52e8481ac62

Access comprehensive regulatory information for "Reted" fiberglass root column (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number de733a9acfbd37a46cf7b52e8481ac62 and manufactured by RTD. 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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de733a9acfbd37a46cf7b52e8481ac62
Registration Details
Taiwan FDA Registration: de733a9acfbd37a46cf7b52e8481ac62
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Device Details

"Reted" fiberglass root column (unsterilized)
TW: "้›ทๆณฐๅพท" ็Žป็’ƒ็บ–็ถญ็‰™ๆ นๆŸฑ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

de733a9acfbd37a46cf7b52e8481ac62

DHA04401302201

Company Information

France

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Center Column Nail (F3810)".

F Dentistry

F.3810 Root canal center post

import

Dates and Status

May 16, 2013

May 16, 2028